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109544-39-0

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109544-39-0 Usage

General Description

The chemical 5-(Chloromethyl)-2-(4-chlorophenyl)-4-methyloxazole is a heterocyclic compound with a chloromethyl group, a 4-chlorophenyl group, and a methyl group attached to an oxazole ring. It is often used as a building block in the synthesis of pharmaceutical drugs and agrochemicals. 5-(CHLOROMETHYL)-2-(4-CHLOROPHENYL)-4-METHYLOXAZOLE has potential use as an antimicrobial and antifungal agent due to its oxazole structure, which has been shown to exhibit bioactive properties. It is important to handle this compound carefully, as chloromethyl groups can be toxic and potentially carcinogenic.

Check Digit Verification of cas no

The CAS Registry Mumber 109544-39-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,5,4 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 109544-39:
(8*1)+(7*0)+(6*9)+(5*5)+(4*4)+(3*4)+(2*3)+(1*9)=130
130 % 10 = 0
So 109544-39-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H9Cl2NO/c1-7-10(6-12)15-11(14-7)8-2-4-9(13)5-3-8/h2-5H,6H2,1H3

109544-39-0SDS

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 5-(chloromethyl)-2-(4-chlorophenyl)-4-methyl-1,3-oxazole

1.2 Other means of identification

Product number -
Other names 2-(4-chlorophenyl)-4-methyl-5-chloromethyloxazole

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:109544-39-0 SDS

109544-39-0Downstream Products

109544-39-0Relevant articles and documents

A new approach to the synthesis of 2-aryl-4-halomethyl-5-methyl-1,3- oxazoles by highly regioselective direct halogenation with NBS or NCS/MeCN

Yamane, Taihei,Mitsudera, Hiroyuki,Shundoh, Takatsugu

, p. 2825 - 2832 (2007/10/03)

A simple and efficient method for the synthesis of 2-aryl-4-bromomethyl-5- methyl-1,3-oxazoles 2 and 2-aryl-4-chloromethyl-5-methyl-1,3-oxazoles 3 is described. The reaction of 2-aryl-4,5-dimethyl-1,3-oxazoles 1 with N-bromosuccinimide and N-chlorosuccini

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