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152120-66-6

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152120-66-6 Usage

General Description

5-(tert-butyldimethylsilyl)-1-methyl-1H-tetrazole is a chemical compound with the molecular formula C9H21N3Si. It is a tetrazole derivative that is often used as a building block in organic synthesis. 5-(TERT-BUTYLDIMETHYLSILYL)-1-METHYL-1H& is a white solid with a molecular weight of 199.37 g/mol. It is commonly used in the pharmaceutical industry and as a reagent in organic chemistry reactions. The tert-butyldimethylsilyl (TBDMS) group is a common protecting group for alcohols, amines, and other functional groups in organic synthesis. Its properties make it a versatile and useful compound for a variety of chemical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 152120-66-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,1,2 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 152120-66:
(8*1)+(7*5)+(6*2)+(5*1)+(4*2)+(3*0)+(2*6)+(1*6)=86
86 % 10 = 6
So 152120-66-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H11BrO/c14-12-6-8-13(9-7-12)15-10-11-4-2-1-3-5-11/h1-9H,10H2

152120-66-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl-dimethyl-(3-methylimidazol-4-yl)silane

1.2 Other means of identification

Product number -
Other names 1H-Imidazole,5-[(1,1-dimethylethyl)dimethylsilyl]-1-methyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:152120-66-6 SDS

152120-66-6Downstream Products

152120-66-6Relevant articles and documents

SYNTHESIS OF 2,5-DILITHIO-1-METHYLIMIDAZOLE

Shapiro, Gideon,Marzi, Martin

, p. 3401 - 3404 (1993)

C5 to C2 position migrations of 2-trialkylsilyl and thiophenyl groups have been observed upon lithiation at the C5-position of corresponding C2-substituted 1-methylimidazoles.Double bromine-lithium exchange of 1-methyl-2,5-dibromoimidazole (5) affords a facile, quantitative and unequivocal synthesis of 2,5-dilithio-1-methyl-imidazole (4).Reaction of 4 with one equivalent of DMF occurs selectively at the C5 position to give 1-methylimidazole-5-carboxaldehyde.

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