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Sigma-Aldrich

Benzylphosphonic acid

97%

Synonym(s):

Phenylmethylphosphonic acid

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About This Item

Empirical Formula (Hill Notation):
C7H9O3P
CAS Number:
6881-57-8
Molecular Weight:
172.12
MDL number:
MFCD00039519
UNSPSC Code:
12352300
PubChem Substance ID:
329765238

Assay

97%

form

solid

mp

173-178 °C

SMILES string

OP(O)(=O)Cc1ccccc1

InChI

1S/C7H9O3P/c8-11(9,10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,8,9,10)

InChI key

OGBVRMYSNSKIEF-UHFFFAOYSA-N

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Nadine Borg et al.
Circulation, 136(3), 297-313 (2017-04-23)
T cells are required for proper healing after myocardial infarction. The mechanism of their beneficial action, however, is unknown. The proinflammatory danger signal ATP, released from damaged cells, is degraded by the ectonucleotidases CD39 and CD73 to the anti-inflammatory mediator
Organic-inorganic nanocomposites by placing conjugated polymers in intimate contact with quantum rods.
Lei Zhao et al.
Advanced materials (Deerfield Beach, Fla.), 23(25), 2844-2849 (2011-05-19)
Alejandra Duarte et al.
PloS one, 7(9), e45829-e45829 (2012-10-03)
Although the contribution of mitochondrial dynamics (a balance in fusion/fission events and changes in mitochondria subcellular distribution) to key biological process has been reported, the contribution of changes in mitochondrial fusion to achieve efficient steroid production has never been explored.
C Poderoso et al.
Endocrine research, 28(4), 413-417 (2003-01-18)
A key regulatory step in the steroidogenic hormones signaling pathway is the synthesis of steroidogenic acute regulatory protein (StAR). This protein facilitates the delivery of cholesterol to the inner mitochondrial membrane, the rate-limiting step in steroidogenesis. ACTH and LH pathway
Andriy I Vovk et al.
Bioorganic & medicinal chemistry letters, 18(16), 4620-4623 (2008-08-02)
The inhibition effects of enantiomerically pure alpha-(N-benzylamino)benzylphosphonic acids and their derivatives on human prostatic acid phosphatase have been investigated. As expected, (R)-alpha-(N-benzylamino)benzylphosphonic acid demonstrated higher affinity for the enzyme than (S)-enantiomer. At the same time, (1R,2S)-phenyl[(1-phenylethyl)amino]methylphosphonic acid was found to
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