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You Searched For: 2-(Hydroxymethyl)phenylboronic+acid+cyclic+monoester


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2-(Hydroxymethyl)phenylboronic acid cyclic monoester

Supplier: TCI America
Description: CAS Number: 5735-41-1
MDL Number: MFCD01075677
Molecular Formula: C7H7BO2
Molecular Weight: 133.94
Form: Crystal
Color: White
Melting point (°C): 98

SDS

Image Unavailable-TCA2559-1G

5-Amino-2-(hydroxymethyl)phenylboronic acid cyclic monoester ≥95.0% (by HPLC, titration analysis)

Catalog Number: (TCA2559-1G)
Supplier: TCI America
Description: 5-Amino-2-(hydroxymethyl)phenylboronic Acid Cyclic Monoester, Purity: >95.0%(HPLC)(T), Cas number: 117098-94-9, Molecular Formula: C7H8BNO2, Molecular Weight: 148.96, Synonyms: 6-Amino-1,3-dihydro-1-hydroxy-2,1-benzoxaborole, Size: 1G

SDS


Image Unavailable-TCH1204-5G

4-(Hydroxymethyl)phenylboronic acid (contains varying amounts of Anhydride)

Supplier: TCI America
Description: CAS Number: 59016-93-2
MDL Number: MFCD00792672
Molecular Formula: C7H9BO3
Molecular Weight: 151.96
Form: Crystal
Color: White

SDS

Image Unavailable-TCH1244-1G

3-(Hydroxymethyl)phenylboronic acid (contains varying amounts of Anhydride)

Supplier: TCI America
Description: CAS Number: 87199-15-3
MDL Number: MFCD01317846
Molecular Formula: C7H9BO3
Molecular Weight: 151.96
Form: Crystal
Color: White
Melting point (°C): 99

SDS

Image Unavailable-TCH1345-1G

2-(Hydroxymethyl)phenylboronic acid (contains varying amounts of Anhydride)

Supplier: TCI America
Description: CAS Number: 87199-14-2
MDL Number: MFCD02258966
Molecular Formula: C7H9BO3
Molecular Weight: 151.96
Form: Crystal
Color: White

SDS Certificates

Image Unavailable-CAAAAL15194-03

4-(Hydroxymethyl)phenylboronic acid 98%

Supplier: Thermo Scientific Chemicals
Description: 4-(Hydroxymethyl)phenylboronic acid 98%

Certificates

Image Unavailable-TCF1090-1G

4-Fluoro-3-(hydroxymethyl)benzeneboronic acid (contains varying amounts of Anhydride)

Supplier: TCI America
Description: 4-Fluoro-3-(hydroxymethyl)phenylboronic Acid, CAS Number: 481681-02-1, Molecular Formula: C7H8BFO3, MW: 169.95, Synonyms: 4-Fluoro-3-(hydroxymethyl)benzeneboronic Acid (contains varying amounts of Anhydride), Size: 200MG

Image Unavailable-TCT3496-5G

4-(Hydroxymethyl)phenylboronic acid pinacol ester ≥98.0% (by GC, titration analysis)

Supplier: TCI America
Description: 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl Alcohol, Purity: >98.0%(GC)(T), CAS Number: 302348-51-2, Molecular Formula: C13H19BO3, Molecular Weight: 234.10, Size: 1G

Certificates

Image Unavailable-TCM0512-025ML

2-Hydroxypropyl methacrylate (mixture of isomers) ≥97.0% stabilized

Supplier: TCI America
Description: (stabilized with MEHQ)

SDS Certificates

Product Image-89357-962

Anti-ACP2 Rabbit Polyclonal Antibody

Catalog Number: (89357-962)
Supplier: Genetex
Description: This gene encodes the beta subunit of lysosomal acid phosphatase (LAP). LAP is chemically and genetically distinct from red cell acid phosphatase. The encoded protein belongs to a family of distinct isoenzymes which hydrolyze orthophosphoric monoesters to alcohol and phosphate. Mutations in this gene or in the related alpha subunit gene cause acid phosphatase deficiency. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq]
Image Unavailable-10486-954

Anti-PXYLP1 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (10486-954)
Supplier: Bioss
Description: ACLP2 (acid phosphatase-like 2), also known as UNQ370 or PRO706, is a 480 amino acid secreted protein that functions to catalyze the H2O-dependent conversion of a phosphate monoester to an alcohol and a phosphate. Expressed as two alternatively spliced isoforms, ACPL2 is encoded by a gene that maps to chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
Product Image-10108-764

Anti-ACP1 Rabbit Polyclonal Antibody

Catalog Number: (10108-764)
Supplier: Prosci
Description: ACP1 belongs to the phosphotyrosine protein phosphatase family of proteins. It functions as an acid phosphatase and a protein tyrosine phosphatase by hydrolyzing protein tyrosine phosphate to protein tyrosine and orthophosphate. This enzyme also hydrolyzes orthophosphoric monoesters to alcohol and orthophosphate.The product of this gene belongs to the phosphotyrosine protein phosphatase family of proteins. It functions as an acid phosphatase and a protein tyrosine phosphatase by hydrolyzing protein tyrosine phosphate to protein tyrosine and orthophosphate. This enzyme also hydrolyzes orthophosphoric monoesters to alcohol and orthophosphate. This gene is genetically polymorphic, and three common alleles segregating at the corresponding locus give rise to six phenotypes. Each allele appears to encode at least two electrophoretically different isozymes, Bf and Bs, which are produced in allele-specific ratios. Three transcript variants encoding distinct isoforms have been identified for this gene.
Image Unavailable-76110-490

Anti-ACPL2 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76110-490)
Supplier: Bioss
Description: ACLP2 (acid phosphatase-like 2), also known as UNQ370 or PRO706, is a 480 amino acid secreted protein that functions to catalyze the H2O-dependent conversion of a phosphate monoester to an alcohol and a phosphate. Expressed as two alternatively spliced isoforms, ACPL2 is encoded by a gene that maps to chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
Product Image-10109-378

Anti-PTPN1 Rabbit Polyclonal Antibody

Catalog Number: (10109-378)
Supplier: Prosci
Description: PTPN1 is the founding member of the protein tyrosine phosphatase (PTP) family. PTPs catalyze the hydrolysis of the phosphate monoesters specifically on tyrosine residues. Members of the PTP family share a highly conserved catalytic motif, which is essential for the catalytic activity. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP has been shown to act as a negative regulator of insulin signaling by dephosphorylating the phosphotryosine residues of insulin receptor kinase. This PTP was also reported to dephosphorylate epidermal growth factor receptor kinase, as well as JAK2 and TYK2 kinases, which implicated the role of this PTP in cell growth control, and cell response to interferon stimulation.The protein encoded by this gene is the founding member of the protein tyrosine phosphatase (PTP) family, which was isolated and identified based on its enzymatic activity and amino acid sequence. PTPs catalyze the hydrolysis of the phosphate monoesters specifically on tyrosine residues. Members of the PTP family share a highly conserved catalytic motif, which is essential for the catalytic activity. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP has been shown to act as a negative regulator of insulin signaling by dephosphorylating the phosphotryosine residues of insulin receptor kinase. This PTP was also reported to dephosphorylate epidermal growth factor receptor kinase, as well as JAK2 and TYK2 kinases, which implicated the role of this PTP in cell growth control, and cell response to interferon stimulation. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Image Unavailable-10486-958

Anti-PXYLP1 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (10486-958)
Supplier: Bioss
Description: ACLP2 (acid phosphatase-like 2), also known as UNQ370 or PRO706, is a 480 amino acid secreted protein that functions to catalyze the H2O-dependent conversion of a phosphate monoester to an alcohol and a phosphate. Expressed as two alternatively spliced isoforms, ACPL2 is encoded by a gene that maps to chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
Image Unavailable-10486-956

Anti-PXYLP1 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10486-956)
Supplier: Bioss
Description: ACLP2 (acid phosphatase-like 2), also known as UNQ370 or PRO706, is a 480 amino acid secreted protein that functions to catalyze the H2O-dependent conversion of a phosphate monoester to an alcohol and a phosphate. Expressed as two alternatively spliced isoforms, ACPL2 is encoded by a gene that maps to chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
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