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114552-32-8

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114552-32-8 Usage

General Description

"(2-Trimethylstannanyl-phenyl)-carbamic acid tert-butyl ester" is a chemical compound with the formula C14H23NO2Sn. It is a white solid with a molecular weight of 356.09 g/mol. (2-TRIMETHYLSTANNANYL-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER is used in the synthesis of various organic and organometallic compounds. It serves as a versatile building block in organic chemistry and can be used in the production of pharmaceuticals, agrochemicals, and other fine chemicals. The tert-butyl ester group provides stability to the compound and allows for easy handling and storage. Additionally, the trimethylstannanyl group can participate in a variety of reactions, making it a valuable tool for chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 114552-32-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,5,5 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 114552-32:
(8*1)+(7*1)+(6*4)+(5*5)+(4*5)+(3*2)+(2*3)+(1*2)=98
98 % 10 = 8
So 114552-32-8 is a valid CAS Registry Number.

114552-32-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(2-trimethylstannylphenyl)carbamate

1.2 Other means of identification

Product number -
Other names (2-trimethylstannanyl-phenyl)-carbamic acid tert-butyl ester

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:114552-32-8 SDS

114552-32-8Relevant articles and documents

In-Cell Generation of Anticancer Phenanthridine Through Bioorthogonal Cyclization in Antitumor Prodrug Development

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, p. 24043 - 24047 (2021/10/07)

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