Cas 1392149-63-1,(3R)-tert-butyl 3-(2-(4-fluorophenyl)-2-oxoethyl)3-hydroxy-2-oxo-2,3-dihydro-1H-indoline-1-carboxylate

1392149-63-1

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Basic information

Product Name: (3R)-tert-butyl 3-(2-(4-fluorophenyl)-2-oxoethyl)3-hydroxy-2-oxo-2,3-dihydro-1H-indoline-1-carboxylate
Synonyms: (3R)-tert-butyl 3-(2-(4-fluorophenyl)-2-oxoethyl)3-hydroxy-2-oxo-2,3-dihydro-1H-indoline-1-carboxylate
CAS NO:1392149-63-1
Molecular Formula:
Molecular Weight: 385.392
EINECS: N/A
Product Categories: N/A
Mol File: 1392149-63-1.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: (3R)-tert-butyl 3-(2-(4-fluorophenyl)-2-oxoethyl)3-hydroxy-2-oxo-2,3-dihydro-1H-indoline-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (3R)-tert-butyl 3-(2-(4-fluorophenyl)-2-oxoethyl)3-hydroxy-2-oxo-2,3-dihydro-1H-indoline-1-carboxylate(1392149-63-1)
EPA Substance Registry System: (3R)-tert-butyl 3-(2-(4-fluorophenyl)-2-oxoethyl)3-hydroxy-2-oxo-2,3-dihydro-1H-indoline-1-carboxylate(1392149-63-1)

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: 1392149-63-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1392149-63-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,1,4 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1392149-63:
(9*1)+(8*3)+(7*9)+(6*2)+(5*1)+(4*4)+(3*9)+(2*6)+(1*3)=171
171 % 10 = 1
So 1392149-63-1 is a valid CAS Registry Number.

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1392149-63-1Relevant articles and documents

Enantioselective decarboxylative aldol addition of β-ketoacids to isatins catalyzed by binaphthyl-modified organocatalyst

Suh, Chang Won,Chang, Chul Woo,Choi, Keon Woong,Lim, Young Jo,Kim, Dae Young

, p. 3651 - 3654 (2013/07/05)

The catalytic enantioselective decarboxylative aldol addition reaction of isatins with β-ketoacids promoted by chiral bifunctional organocatalysts have been developed, allowing facile synthesis of the corresponding chiral 3-hydroxy-3-phenacyloxindole deri

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