39812-29-8 Usage
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.
Uses
Used in Organic Synthesis:
[3-CHLORO-3-(4-METHOXYPHENYL)PROP-2-ENYLIDENE](DIMETHYL)AMMONIUM PERCHLORATE is used as a reactant for the synthesis of more complex organic molecules, particularly due to the presence of the chloro and methoxy substituents on the phenyl ring.
Used in Chemical Research:
[3-CHLORO-3-(4-METHOXYPHENYL)PROP-2-ENYLIDENE](DIMETHYL)AMMONIUM PERCHLORATE is also utilized in chemical research to study its properties and potential applications in various fields.
Used in Pharmaceutical Industry:
[3-CHLORO-3-(4-METHOXYPHENYL)PROP-2-ENYLIDENE](DIMETHYL)AMMONIUM PERCHLORATE has potential applications in the pharmaceutical industry, where it may serve as a building block for the development of new drugs.
Used in Dyes Industry:
Additionally, this compound may be used in the dyes industry for the creation of new dye products.
Safety Precautions:
It is important to handle [3-CHLORO-3-(4-METHOXYPHENYL)PROP-2-ENYLIDENE](DIMETHYL)AMMONIUM PERCHLORATE with caution due to its potential reactivity and toxicity. Proper safety measures should be taken during its use in any application.
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.
39812-29-8Relevant 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