2,2-Diphenylacetic acid
2,2-Diphenylacetic acid Basic information
- Product Name:
- 2,2-Diphenylacetic acid
- Synonyms:
-
- MONOCARBOXYMETHANEDIPHENYL
- RARECHEM AL BO 1083
- A-PHENYLPHENYLACETIC ACID
- CARBOXYMETHANEDIPHENYL
- DIPHENYLACETIC ACID
- DIPHENYLMETHANE-A-CARBOXYLIC ACID
- DIPHENYLMETHANE-ALPHA-CARBOXYLIC ACID
- DIPHENYLMETHANECARBOXYLIC ACID
- CAS:
- 117-34-0
- MF:
- C14H12O2
- MW:
- 212.24
- EINECS:
- 204-185-0
- Product Categories:
-
- C13 to C42+
- Pharmaceutical Intermediates
- Aromatic Phenylacetic Acids and Derivatives
- C13 to C42+Alphabetic
- Carbonyl Compounds
- Carboxylic Acids
- D
- DIO - DIZ
- Mol File:
- 117-34-0.mol
2,2-Diphenylacetic acid Chemical Properties
- Melting point:
- 147-149 °C(lit.)
- Boiling point:
- 195°C 25mm
- Density
- 1,257 g/cm3
- vapor pressure
- 0.001Pa at 25℃
- refractive index
- 1.6000 (estimate)
- Flash point:
- 195°C/25mm
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- 0.13g/l
- form
- Crystalline Powder
- pka
- 3.94(at 25℃)
- color
- White to creamy-white
- PH
- 3.8 (H2O, 20℃)(saturated solution)
- Water Solubility
- Slightly soluble in water(0.13g/L).
- Merck
- 14,3316
- BRN
- 1910978
- InChIKey
- PYHXGXCGESYPCW-UHFFFAOYSA-N
- LogP
- 3.17 at 25℃
- CAS DataBase Reference
- 117-34-0(CAS DataBase Reference)
- NIST Chemistry Reference
- Benzeneacetic acid, «alpha»-phenyl-(117-34-0)
- EPA Substance Registry System
- Benzeneacetic acid, .alpha.-phenyl- (117-34-0)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/38-36/37/38
- Safety Statements
- 24/25-36/37-26
- WGK Germany
- 2
- RTECS
- AH2515000
- TSCA
- Yes
- HazardClass
- IRRITANT
- HS Code
- 29163900
- Toxicity
- mouse,LD50,intraperitoneal,500mg/kg (500mg/kg),Farmaco, Edizione Scientifica. Vol. 13, Pg. 286, 1958.
MSDS
- Language:English Provider:2,2-Diphenylacetic acid
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
2,2-Diphenylacetic acid Usage And Synthesis
Chemical Properties
white to creamy-white crystalline powder
Uses
Kinetic resolution of racemic 1-heteroarylalkanols by asymmetric esterification using diphenylacetic acid with pivalic anhydride and a chiral acyl-transfer catalyst is described. Molecular crystal of acridine and diphenylacetic acid and its absolute asymmetric photodecarboxylating condensation generates chirality in a two-component. The activation parameters for the racemization of a series of ortho-alkyl-substituted diphenylacetic acids are determined.
Definition
ChEBI: A monocarboxylic acid that is acetic acid where the methyl hydrogens have been replaced by two phenyl groups respectively.
Synthesis Reference(s)
Journal of the American Chemical Society, 69, p. 2325, 1947 DOI: 10.1021/ja01202a023
Synthetic Communications, 17, p. 1919, 1987 DOI: 10.1080/00397918708057804
Purification Methods
Crystallise the acid from *benzene, H2O or aqueous 50% EtOH. [Beilstein 9 H 673, 9 IV 2492.]
2,2-Diphenylacetic acid Preparation Products And Raw materials
Raw materials
Preparation Products
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2,2-Diphenylacetic acid(117-34-0)Related Product Information
- Phenylacetic acid
- Phenyl sulfoxide
- 2-Phenylacetophenone
- Triphenylacetic acid
- 2,2-Diphenylglycine
- Propantheline bromide
- 2,2'-DICHLOROBENZILIC ACID
- Adiphenine hydrochloride
- Benzilic acid
- 9-Carboxyfluorene
- Methyl benzilate
- METHANTHELINE BROMIDE
- XANTHENE-9-CARBOXYLIC ACID
- METHYL DIPHENYLACETATE
- BENACTYZINE HYDROCHLORIDE
- ETHYL BENZILATE
- BIS(2,4-DINITROPHENYL)ACETIC ACID ETHYL ESTER
- 2-ETHYLTHIO-2,2-DIPHENYLACETIC ACID