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1094047-97-8

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1094047-97-8 Usage

Chemical structure

Contains a pyrimidine ring with a bromopropyl group attached to it.

Common use

Used as a building block in organic synthesis and pharmaceutical research.

Reactivity

The presence of the bromopropyl group makes the compound useful for various chemical reactions, including nucleophilic substitution and palladium-catalyzed cross-coupling reactions.

Potential applications

Has potential applications in drug development and agrochemical synthesis due to its unique structure and reactivity.

Safety

Handle with caution, as bromine-containing compounds can be harmful if not properly handled.

Check Digit Verification of cas no

The CAS Registry Mumber 1094047-97-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,4,0,4 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1094047-97:
(9*1)+(8*0)+(7*9)+(6*4)+(5*0)+(4*4)+(3*7)+(2*9)+(1*7)=158
158 % 10 = 8
So 1094047-97-8 is a valid CAS Registry Number.

1094047-97-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-bromopropyl)pyrimidine

1.2 Other means of identification

Product number -
Other names -

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:1094047-97-8 SDS

1094047-97-8Upstream product

1094047-97-8Relevant articles and documents

N-alkylation of lactams with secondary heterobenzylic bromides

Yu, Ming,Stevenson, Karis,Zhou, Gene

, p. 5591 - 5594 (2014)

We herein report a general N-alkylation reaction of lactams with secondary heterobenzylic bromides. This methodology features mild reaction condition, moderate to high product isolation yield, and broad substrate scope. Good chemical and structural tolerance has also been demonstrated by both the secondary heterobenzylic bromides and lactam substrates.

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