Cas 1010721-82-0,methyl (E)-2-[(tert-butyl)-(p-tolylsulfonylamino)methyl]-3-(p-tolylsulfonylamino)prop-2-enoate

1010721-82-0

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Basic information

Product Name: methyl (E)-2-[(tert-butyl)-(p-tolylsulfonylamino)methyl]-3-(p-tolylsulfonylamino)prop-2-enoate
Synonyms:
CAS NO:1010721-82-0
Molecular Formula:
Molecular Weight: 494.633
EINECS: N/A
Product Categories: N/A
Mol File: 1010721-82-0.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 (E)-2-[(tert-butyl)-(p-tolylsulfonylamino)methyl]-3-(p-tolylsulfonylamino)prop-2-enoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (E)-2-[(tert-butyl)-(p-tolylsulfonylamino)methyl]-3-(p-tolylsulfonylamino)prop-2-enoate(1010721-82-0)
EPA Substance Registry System: methyl (E)-2-[(tert-butyl)-(p-tolylsulfonylamino)methyl]-3-(p-tolylsulfonylamino)prop-2-enoate(1010721-82-0)

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: 1010721-82-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1010721-82-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,0,7,2 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1010721-82:
(9*1)+(8*0)+(7*1)+(6*0)+(5*7)+(4*2)+(3*1)+(2*8)+(1*2)=80
80 % 10 = 0
So 1010721-82-0 is a valid CAS Registry Number.

1010721-82-0Upstream product

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1010721-82-0Relevant articles and documents

Three-component coupling reaction and cyclization of N-tosylimines and TMS-substituted propiolate mediated by DABCO

Matsuya, Yuji,Hayashi, Kousuke,Wada, Akiho,Nemoto, Hideo

, p. 1987 - 1990 (2008/09/18)

A new three-component coupling reaction of methyl 3- trimethylsilylpropiolate, N-tosylimine, and tosylamide mediated by DABCO was developed. This reaction was based on the consecutive α- and β-activation method of propiolate involving intramolecular silyl

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