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Merck
CN

737887

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

Key Documents

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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

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKCH2491
MKBL7718V
MKBH5802V

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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)
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
D Elias Jesu Packiam et al.
Dalton transactions (Cambridge, England : 2003), 46(46), 16102-16112 (2017-11-11)
Twenty new molybdenum phosphonates and diphosphonates have been synthesized and structurally characterized by single crystal and powder X-ray diffraction, CHN analyses, spectroscopic and thermal studies. Four of them are molecular phenyl- and benzyl-phosphonates containing discrete [(MoO
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.
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