Cas 1370735-35-5,tert-butyl 2-bromo-4-methoxyphenyl(((chloromethyl)dimethylsilyl)methyl)carbamate

1370735-35-5

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Basic information

Product Name: tert-butyl 2-bromo-4-methoxyphenyl(((chloromethyl)dimethylsilyl)methyl)carbamate
Synonyms: tert-butyl 2-bromo-4-methoxyphenyl(((chloromethyl)dimethylsilyl)methyl)carbamate
CAS NO:1370735-35-5
Molecular Formula:
Molecular Weight: 422.822
EINECS: N/A
Product Categories: N/A
Mol File: 1370735-35-5.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: tert-butyl 2-bromo-4-methoxyphenyl(((chloromethyl)dimethylsilyl)methyl)carbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl 2-bromo-4-methoxyphenyl(((chloromethyl)dimethylsilyl)methyl)carbamate(1370735-35-5)
EPA Substance Registry System: tert-butyl 2-bromo-4-methoxyphenyl(((chloromethyl)dimethylsilyl)methyl)carbamate(1370735-35-5)

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: 1370735-35-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1370735-35-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,0,7,3 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1370735-35:
(9*1)+(8*3)+(7*7)+(6*0)+(5*7)+(4*3)+(3*5)+(2*3)+(1*5)=155
155 % 10 = 5
So 1370735-35-5 is a valid CAS Registry Number.

1370735-35-5Upstream product

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1370735-35-5Relevant articles and documents

Intramolecular sila-matteson rearrangement: A general access to silylated heterocycles

Francois, Cyril,Boddaert, Thomas,Durandetti, Muriel,Querolle, Olivier,Van Hijfte, Luc,Meerpoel, Lieven,Angibaud, Patrick,Maddaluno, Jacques

supporting information; experimental part, p. 2074 - 2077 (2012/06/29)

A series of new silylated heterocycles has been efficiently prepared using an intramolecular silicon version of the Matteson rearrangement, providing two isomers of binuclear heterocycles. This method applies to a large variety of substrates, a direct rel

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