Cas 1202888-86-5,methyl (R)-2-{[1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl](4-methoxyphenyl)methyl}acrylate

1202888-86-5

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Basic information

Product Name: methyl (R)-2-{[1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl](4-methoxyphenyl)methyl}acrylate
Synonyms:
CAS NO:1202888-86-5
Molecular Formula:
Molecular Weight: 401.419
EINECS: N/A
Product Categories: N/A
Mol File: 1202888-86-5.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 (R)-2-{[1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl](4-methoxyphenyl)methyl}acrylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (R)-2-{[1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl](4-methoxyphenyl)methyl}acrylate(1202888-86-5)
EPA Substance Registry System: methyl (R)-2-{[1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl](4-methoxyphenyl)methyl}acrylate(1202888-86-5)

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: 1202888-86-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1202888-86-5 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, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1202888-86:
(9*1)+(8*2)+(7*0)+(6*2)+(5*8)+(4*8)+(3*8)+(2*8)+(1*6)=155
155 % 10 = 5
So 1202888-86-5 is a valid CAS Registry Number.

1202888-86-5Upstream product

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1202888-86-5Relevant 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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