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D211605

Sigma-Aldrich

2,2-Diphenylpropionic acid

95%

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About This Item

Linear Formula:
CH3C(C6H5)2CO2H
CAS Number:
5558-66-7
Molecular Weight:
226.27
EC Number:
226-924-6
MDL number:
MFCD00004189
UNSPSC Code:
12352100
PubChem Substance ID:
24893629
NACRES:
NA.22

Quality Level

100

Assay

95%

form

powder

bp

300 °C (lit.)

mp

172-175 °C (lit.)

SMILES string

CC(C(O)=O)(c1ccccc1)c2ccccc2

InChI

1S/C15H14O2/c1-15(14(16)17,12-8-4-2-5-9-12)13-10-6-3-7-11-13/h2-11H,1H3,(H,16,17)

InChI key

ODELFXJUOVNEFZ-UHFFFAOYSA-N

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB0153
STBJ2097
STBJ0960
STBF9396V
S46567

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R K Gordon et al.
Molecular pharmacology, 36(5), 766-772 (1989-11-01)
Quantitative structure-activity relationships between pharmacological activities and physical properties of a series of 2,2-diphenylpropionate compounds were used to define the topography of the antagonist binding site of muscarinic receptors. XICAMM, a computer molecular modeling program, was used to calculate geometrical
T F Holzman et al.
Biochemistry, 20(19), 5524-5528 (1981-09-15)
We have found a new class of inhibitors of the bacterial bioluminescence reaction, the N,N-diphenylalkylamines and acids. We have studied the action of one of these compounds 2,2-diphenylpropylamine. The amine was competitive with the long-chain aliphatic aldehyde substrate (Ki congruent
N Toyomura et al.
Bioscience, biotechnology, and biochemistry, 64(3), 610-612 (2000-05-10)
A variety of 2,2-diphenylpropionate derivatives with an amino substituent were synthesized and their effects on larval growth of the silkworm, Bombyx mori, were examined by dietary administration. Of the compounds tested, 3-(4-ethylpiperazin-1-yl)propyl 2,2-diphenylpropionate (3) caused significant prolongation of the larval

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