Cas 1384468-87-4,(2'S,3R)-methyl 7-bromo-4',4'-dicyano-1-methyl-2-oxo-2'-phenyl-2',4'-dihydrospiro[indoline-3,3'-pyrrole]-2'-carboxylate

1384468-87-4

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Basic information

Product Name: (2'S,3R)-methyl 7-bromo-4',4'-dicyano-1-methyl-2-oxo-2'-phenyl-2',4'-dihydrospiro[indoline-3,3'-pyrrole]-2'-carboxylate
Synonyms:
CAS NO:1384468-87-4
Molecular Formula:
Molecular Weight: 463.29
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: (2'S,3R)-methyl 7-bromo-4',4'-dicyano-1-methyl-2-oxo-2'-phenyl-2',4'-dihydrospiro[indoline-3,3'-pyrrole]-2'-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2'S,3R)-methyl 7-bromo-4',4'-dicyano-1-methyl-2-oxo-2'-phenyl-2',4'-dihydrospiro[indoline-3,3'-pyrrole]-2'-carboxylate(1384468-87-4)
EPA Substance Registry System: (2'S,3R)-methyl 7-bromo-4',4'-dicyano-1-methyl-2-oxo-2'-phenyl-2',4'-dihydrospiro[indoline-3,3'-pyrrole]-2'-carboxylate(1384468-87-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1384468-87-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1384468-87-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,4,6 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1384468-87:
(9*1)+(8*3)+(7*8)+(6*4)+(5*4)+(4*6)+(3*8)+(2*8)+(1*7)=204
204 % 10 = 4
So 1384468-87-4 is a valid CAS Registry Number.

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1384468-87-4Relevant academic research and scientific papers

Enantioselective synthesis of 3,3′-dihydropyrryl-spirooxindoles via an organocatalytic three-component reaction

Wei, Wen-Tao,Chen, Chun-Xia,Lu, Rui-Jiong,Wang, Jin-Jia,Zhang, Xue-Jing,Yan, Ming

experimental part, p. 5245 - 5252 (2012/08/07)

An organocatalytic three-component reaction of isatins, malononitrile and isocyanoacetates provided 3,3′-dihydropyrryl-spirooxindoles in excellent yields and enantioselectivities. The products could be readily converted to valuable 3,3′-pyrrolidinyl-spiro

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