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39812-29-8

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39812-29-8 Usage

General Description

[3-CHLORO-3-(4-METHOXYPHENYL)PROP-2-ENYLIDENE](DIMETHYL)AMMONIUM PERCHLORATE is a chemical compound with the molecular formula C13H16ClN2O5ClO4. It is a perchlorate salt that contains a quaternary ammonium cation and a substituted cinnamaldehyde anion. [3-CHLORO-3-(4-METHOXYPHENYL)PROP-2-ENYLIDENE](DIMETHYL)AMMONIUM PERCHLORATE is often used as a reactant in organic synthesis and chemical research. It has potential applications in pharmaceuticals, dyes, and other industrial processes. The presence of the chloro and methoxy substituents on the phenyl ring makes this compound a useful building block for the synthesis of more complex organic molecules. However, it is important to handle this compound with caution due to its potential reactivity and toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 39812-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,1 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 39812-29:
(7*3)+(6*9)+(5*8)+(4*1)+(3*2)+(2*2)+(1*9)=138
138 % 10 = 8
So 39812-29-8 is a valid CAS Registry Number.

39812-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-chloro-3-(4-methoxyphenyl)-2-propen-1-yliden] dimethyliminium perchlorate

1.2 Other means of identification

Product number -
Other names [3-chloro-3-(4-methoxy-phenyl)-allylidene]-dimethyl-ammonium, perchlorate

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:39812-29-8 SDS

39812-29-8Relevant articles and documents

New Synthesis of Isoxazoles and Isothiazoles. A Convenient Synthesis of Thioenaminones from Enaminones

Lin, Yang-i,Lang, Stanley, A.

, p. 4857 - 4860 (2007/10/02)

The reaction of 1-aryl-3-(dimethylamino)-2-propene-1-ones (enaminones) and 1-aryl-3-(dimethylamino)-2-propene-1-thiones (thioenaminones) with hydroxylamine-O-sulfonic acid gave, respectively, isoxazoles in 76-84 percent yields and isothiazoles in 60-65 pe

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