Cas 1042728-32-4,1-(bis(trimethylsilyl)methyl)-3-(3-methoxyphenyl)-1-methylurea

1042728-32-4

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Basic information

Product Name: 1-(bis(trimethylsilyl)methyl)-3-(3-methoxyphenyl)-1-methylurea
Synonyms: 1-(bis(trimethylsilyl)methyl)-3-(3-methoxyphenyl)-1-methylurea
CAS NO:1042728-32-4
Molecular Formula:
Molecular Weight: 338.597
EINECS: N/A
Product Categories: N/A
Mol File: 1042728-32-4.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: 1-(bis(trimethylsilyl)methyl)-3-(3-methoxyphenyl)-1-methylurea(CAS DataBase Reference)
NIST Chemistry Reference: 1-(bis(trimethylsilyl)methyl)-3-(3-methoxyphenyl)-1-methylurea(1042728-32-4)
EPA Substance Registry System: 1-(bis(trimethylsilyl)methyl)-3-(3-methoxyphenyl)-1-methylurea(1042728-32-4)

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: 1042728-32-4(Hazardous Substances Data)

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1042728-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1042728-32-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,2,7,2 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1042728-32:
(9*1)+(8*0)+(7*4)+(6*2)+(5*7)+(4*2)+(3*8)+(2*3)+(1*2)=124
124 % 10 = 4
So 1042728-32-4 is a valid CAS Registry Number.

1042728-32-4Upstream product

1042728-32-4Downstream Products

591-63-9 n-butyl crotonate

1042728-32-4Relevant articles and documents

Catalytic amide-mediated methyl transfer from silanes to alkenes in Fujiwara-Moritani oxidative coupling

Rauf, Waqar,Brown, John M.

, p. 4228 - 4230 (2008)

(Chemical Equation Presented) Intramolecular assistance: Carbon-bound trimethylsilyl groups are activated intramolecularly by a carbonyl group and can participate in Heck reactions under oxidative conditions. Good stereoselectivities are obtained for a range of di-and trisubstituted alkenes (see example).

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