Cas 876337-70-1,1H-Indole-3-carboxylic acid, 2,3-dihydro-1,3-dimethyl-2-oxo-, phenyl ester, (3S)-

876337-70-1

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Basic information

Product Name: 1H-Indole-3-carboxylic acid, 2,3-dihydro-1,3-dimethyl-2-oxo-, phenyl ester, (3S)-
Synonyms:
CAS NO:876337-70-1
Molecular Formula: C17H15NO3
Molecular Weight: 281.311
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: 1H-Indole-3-carboxylic acid, 2,3-dihydro-1,3-dimethyl-2-oxo-, phenyl ester, (3S)-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Indole-3-carboxylic acid, 2,3-dihydro-1,3-dimethyl-2-oxo-, phenyl ester, (3S)-(876337-70-1)
EPA Substance Registry System: 1H-Indole-3-carboxylic acid, 2,3-dihydro-1,3-dimethyl-2-oxo-, phenyl ester, (3S)-(876337-70-1)

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: 876337-70-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 876337-70-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,3,3 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 876337-70:
(8*8)+(7*7)+(6*6)+(5*3)+(4*3)+(3*7)+(2*7)+(1*0)=211
211 % 10 = 1
So 876337-70-1 is a valid CAS Registry Number.

876337-70-1Upstream product

876337-62-1 carbonic acid 1,3-dimethyl-1H-indol-2-yl ester phenyl ester

876337-70-1Downstream Products

876337-70-1Relevant academic research and scientific papers

Chiral bicycle imidazole nucleophilic catalysts: Rational design, facile synthesis, and successful application in asymmetric Steglich rearrangement

Zhang, Zhenfeng,Xie, Fang,Jia, Jia,Zhang, Wanbin

, p. 15939 - 15941 (2010)

A new type of chiral bicycle imidazole nucleophilic catalyst was rationally designed, facilely synthesized, and successfully applied in an asymmetric Steglich rearrangement with good to excellent yield and enantioselectivity at ambient temperature. Moreov

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