A3162312
Diphenylacetic acid , 98% , 117-34-0
CAS NO.:117-34-0
Empirical Formula: C14H12O2
Molecular Weight: 212.24
MDL number: MFCD00004251
EINECS: 204-185-0
Pack Size | Price | Stock | Quantity |
25G | RMB37.60 | In Stock |
|
100G | RMB88.80 | In Stock |
|
250g | RMB215.20 | In Stock |
|
500G | RMB428.80 | In Stock |
|
others | Enquire |
Update time: 2022-07-08
PRODUCT 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 |
pka | 3.94(at 25℃) |
form | Crystalline Powder |
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) |
Description and 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.
Safety
Symbol(GHS) | GHS07 |
Signal word | Warning |
Hazard statements | H302-H319-H412 |
Precautionary statements | P264-P270-P273-P280-P301+P312-P305+P351+P338 |
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. |