Cas 1202888-98-9,methyl (S)-2-[(2-chlorophenyl)(4,5,6,7-tetrachloro-1,3-dioxoisoindolin-2-yl)methyl]acrylate

1202888-98-9

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Basic information

Product Name: methyl (S)-2-[(2-chlorophenyl)(4,5,6,7-tetrachloro-1,3-dioxoisoindolin-2-yl)methyl]acrylate
Synonyms:
CAS NO:1202888-98-9
Molecular Formula:
Molecular Weight: 493.558
EINECS: N/A
Product Categories: N/A
Mol File: 1202888-98-9.mol
Article Data: 1

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: methyl (S)-2-[(2-chlorophenyl)(4,5,6,7-tetrachloro-1,3-dioxoisoindolin-2-yl)methyl]acrylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (S)-2-[(2-chlorophenyl)(4,5,6,7-tetrachloro-1,3-dioxoisoindolin-2-yl)methyl]acrylate(1202888-98-9)
EPA Substance Registry System: methyl (S)-2-[(2-chlorophenyl)(4,5,6,7-tetrachloro-1,3-dioxoisoindolin-2-yl)methyl]acrylate(1202888-98-9)

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: 1202888-98-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1202888-98-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,8,8 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1202888-98:
(9*1)+(8*2)+(7*0)+(6*2)+(5*8)+(4*8)+(3*8)+(2*9)+(1*8)=159
159 % 10 = 9
So 1202888-98-9 is a valid CAS Registry Number.

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1202888-98-9Relevant articles and documents

Enantioselective allylic amination of morita - baylis - hillman carbonates catalysed by modified cinchona alkaloids

Zhang, Shan-Jun,Cui, Hai-Lei,Jiang, Kun,Li, Rui,Ding, Zhen-Yu,Chen, Ying-Chun

experimental part, p. 5804 - 5809 (2010/03/03)

An efficient procedure for the asymmetric allylic amination of Morita - Baylis - Hillman carbonates with cyclic imides catalysed by commercially available cinchona alkaloids is reported. It proves to be a facile protocol that affords α-methylene β-amino e

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