Cas 114155-18-9,3,3,3-Trifluoro-2-hydroxy-2-(2-phenyl-1H-indol-3-yl)-propionic acid methyl ester

114155-18-9

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Basic information

Product Name: 3,3,3-Trifluoro-2-hydroxy-2-(2-phenyl-1H-indol-3-yl)-propionic acid methyl ester
Synonyms: 3,3,3-Trifluoro-2-hydroxy-2-(2-phenyl-1H-indol-3-yl)-propionic acid methyl ester
CAS NO:114155-18-9
Molecular Formula:
Molecular Weight: 349.309
EINECS: N/A
Product Categories: N/A
Mol File: 114155-18-9.mol
Article Data: 2

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3,3,3-Trifluoro-2-hydroxy-2-(2-phenyl-1H-indol-3-yl)-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3,3,3-Trifluoro-2-hydroxy-2-(2-phenyl-1H-indol-3-yl)-propionic acid methyl ester(114155-18-9)
EPA Substance Registry System: 3,3,3-Trifluoro-2-hydroxy-2-(2-phenyl-1H-indol-3-yl)-propionic acid methyl ester(114155-18-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 114155-18-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114155-18-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,1,5 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 114155-18:
(8*1)+(7*1)+(6*4)+(5*1)+(4*5)+(3*5)+(2*1)+(1*8)=89
89 % 10 = 9
So 114155-18-9 is a valid CAS Registry Number.

114155-18-9Upstream product

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114155-18-9Relevant articles and documents

Rapid and convenient synthesis of aryl- and heteroaryl-α-hydroxy- α-trifluoromethyl acetate via Friedel-Crafts alkylation under solvent- and catalyst-free conditions

Zhao, Jun-Ling,Liu, Li,Zhang, Hai-Bo,Wu, Yan-Chao,Wang, Dong,Chen, Yong Jun

, p. 2511 - 2514 (2007/10/03)

Solvent- and catalyst-free Friedel-Crafts alkylation reactions of aromatic and heteroaromatic compounds with methyl trifluoropyruvate (2) were carried out at room temperature and finished in several minutes with good to excellent yields of the addition pr

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