Cas 1318792-15-2,methyl 5-(4,6-dimethylpyrimidin-2-yl)-2-methyl-4-(phenylsulfonyl)pyrrolidine-2-carboxylate

1318792-15-2

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Basic information

Product Name: methyl 5-(4,6-dimethylpyrimidin-2-yl)-2-methyl-4-(phenylsulfonyl)pyrrolidine-2-carboxylate
Synonyms: methyl 5-(4,6-dimethylpyrimidin-2-yl)-2-methyl-4-(phenylsulfonyl)pyrrolidine-2-carboxylate
CAS NO:1318792-15-2
Molecular Formula:
Molecular Weight: 389.475
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: methyl 5-(4,6-dimethylpyrimidin-2-yl)-2-methyl-4-(phenylsulfonyl)pyrrolidine-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 5-(4,6-dimethylpyrimidin-2-yl)-2-methyl-4-(phenylsulfonyl)pyrrolidine-2-carboxylate(1318792-15-2)
EPA Substance Registry System: methyl 5-(4,6-dimethylpyrimidin-2-yl)-2-methyl-4-(phenylsulfonyl)pyrrolidine-2-carboxylate(1318792-15-2)

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: 1318792-15-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1318792-15-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,8,7,9 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1318792-15:
(9*1)+(8*3)+(7*1)+(6*8)+(5*7)+(4*9)+(3*2)+(2*1)+(1*5)=172
172 % 10 = 2
So 1318792-15-2 is a valid CAS Registry Number.

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1318792-15-2Relevant academic research and scientific papers

XY-ZH compounds as potential 1,3-dipoles. Part 65: Atom economic cascade synthesis of highly functionalized pyrimidinylpyrrolidines

Elboray, Elghareeb E.,Grigg, Ronald,Fishwick, Colin W.G.,Kilner, Colin,Sarker, Mohammed A.B.,Aly, Moustafa F.,Abbas-Temirek, Hussien H.

, p. 5700 - 5710 (2011)

The results of the reaction of aminomethyl heterocycles and 4,6-dimethyl-2-formylpyrimidine and of activated secondary amines with different aryl/heteroaryl or aliphatic aldehydes and N-methylmaleimide or maleimide are described. In the former case the re

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