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175393-09-6

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175393-09-6 Usage

General Description

Carbamic acid, (5-bromo-2-pyridinyl)-, phenylmethyl ester is a chemical compound with the molecular formula C12H11BrN2O2. It is an ester of carbamic acid and is derived from 5-bromo-2-pyridinyl and phenylmethanol. Carbamic acid, (5-bromo-2-pyridinyl)-,phenylmethyl ester is commonly used in the pharmaceutical industry as an intermediate in the synthesis of various drugs. It may also have applications in insecticides and fungicides. Due to its potential reactivity and toxicity, proper handling and storage precautions should be taken when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 175393-09-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,3,9 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 175393-09:
(8*1)+(7*7)+(6*5)+(5*3)+(4*9)+(3*3)+(2*0)+(1*9)=156
156 % 10 = 6
So 175393-09-6 is a valid CAS Registry Number.

175393-09-6SDS

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 Benzyl (5-bromopyridin-2-yl)carbamate

1.2 Other means of identification

Product number -
Other names 5-Bromo-2-(Cbz-amino)pyridine

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:175393-09-6 SDS

175393-09-6Downstream Products

175393-09-6Relevant articles and documents

Synthesis of Functionalized 3-Pyridyl Methyl Ketones

Wright,Hageman,McClure

, p. 717 - 723 (2007/10/03)

A synthesis of 3-pyridyl methyl ketones is described that employs a palladium-catalyzed olefination of 3-bromopyridines with butyl vinyl ether followed by acid hydrolysis of the intermediate pyridyl vinyl ether in situ. This method has been applied to bromoquinoline substrates as well. The reaction is compatible with a variety of functional groups.

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