Cas 117291-10-8,3-o-Tolyl-3-(2,2,2-trifluoro-acetylamino)-propionic acid

117291-10-8

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Basic information

Product Name: 3-o-Tolyl-3-(2,2,2-trifluoro-acetylamino)-propionic acid
Synonyms: 3-o-Tolyl-3-(2,2,2-trifluoro-acetylamino)-propionic acid
CAS NO:117291-10-8
Molecular Formula:
Molecular Weight: 275.227
EINECS: N/A
Product Categories: N/A

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-o-Tolyl-3-(2,2,2-trifluoro-acetylamino)-propionic acid(CAS DataBase Reference)
NIST Chemistry Reference: 3-o-Tolyl-3-(2,2,2-trifluoro-acetylamino)-propionic acid(117291-10-8)
EPA Substance Registry System: 3-o-Tolyl-3-(2,2,2-trifluoro-acetylamino)-propionic acid(117291-10-8)

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: 117291-10-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 117291-10-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,2,9 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 117291-10:
(8*1)+(7*1)+(6*7)+(5*2)+(4*9)+(3*1)+(2*1)+(1*0)=108
108 % 10 = 8
So 117291-10-8 is a valid CAS Registry Number.

117291-10-8Upstream product

117291-10-8Downstream Products

117291-27-7 3-o-Tolyl-3-(2,2,2-trifluoro-acetylamino)-propionyl chloride

117291-10-8Relevant academic research and scientific papers

Effective cerebral antihypoxic activity of new aminocyclopentanones

Quermonne,Dallemagne,Louchahi-Raoul,Pilo,Rault,Robba

, p. 961 - 965 (2007/10/02)

Effective antihypoxic activity of new aminocyclopentanones which was higher than that of the reference compounds has been demonstrated by the SCR hypoxia test.

Une synthese simple des premieres amino-3 indanones-1

Rault, Sylvain,Dallemagne, Patrick,Robba, Max

, p. 1079 - 1083 (2007/10/02)

The synthesis of various substituted 3-amino-1-indanones was achieved in five steps starting from corresponding benzaldehydes.

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