1379331-79-9 Usage
Uses
Used in Organic Synthesis:
2-(bromomethyl)-6-chlorobenzaldehyde is used as a reagent in organic synthesis for the preparation of a variety of organic compounds. Its unique structure allows it to be a key component in creating complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-(bromomethyl)-6-chlorobenzaldehyde is utilized as an intermediate. Its role is crucial in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Agrochemical Production:
Similarly, in agrochemicals, 2-(bromomethyl)-6-chlorobenzaldehyde serves as an intermediate, playing a part in the creation of compounds used in agricultural applications to protect crops and enhance yields.
Used in Fine Chemicals:
2-(bromomethyl)-6-chlorobenzaldehyde is also used in the production of fine chemicals, where its specific properties are harnessed to create high-quality specialty chemicals for various applications.
Used in Medicine and Biotechnology:
Due to its reactivity, 2-(bromomethyl)-6-chlorobenzaldehyde has potential applications in medicine and biotechnology. It can be involved in the development of new treatments and technologies, taking advantage of its chemical versatility.
Check Digit Verification of cas no
The CAS Registry Mumber 1379331-79-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,9,3,3 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1379331-79:
(9*1)+(8*3)+(7*7)+(6*9)+(5*3)+(4*3)+(3*1)+(2*7)+(1*9)=189
189 % 10 = 9
So 1379331-79-9 is a valid CAS Registry Number.
1379331-79-9Relevant academic research and scientific papers
Synthesis of 2-aryl-1,2-dihydrophthalazines via reaction of 2-(bromomethyl)benzaldehydes with arylhydrazines
Aljaar, Nayyef,Conrad, Jürgen,Beifuss, Uwe
, p. 1045 - 1053 (2013/03/29)
The reaction of 2-(bromomethyl)benzaldehydes with arylhydrazines employing K2CO3 as a base and FeCl3 as a catalyst in CH3CN at 100 C delivers 2-aryl-1,2-dihydrophthalazines with yields ranging from 60 to 91%. The transformation is considered to proceed as an intermolecular condensation/intramolecular nucleophilic substitution.
