77072-00-5 Usage
Description
3-(Chloromethyl)-benzaldehyde is a chemical compound that features a benzene ring with a carbonyl group and a chloromethyl group attached at the 3-position. This structure endows it with versatile reactivity and utility in organic synthesis.
Uses
Used in Pharmaceutical Industry:
3-(Chloromethyl)-benzaldehyde is used as a synthetic intermediate for the development of various pharmaceuticals. Its chloromethyl group allows for the creation of new chemical entities through nucleophilic substitution and metal-catalyzed cross-coupling reactions, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 3-(Chloromethyl)-benzaldehyde is utilized as a building block in the synthesis of agrochemicals. Its reactivity enables the production of compounds that can be used in pest control and crop protection, enhancing agricultural productivity.
Used in Dye Industry:
3-(Chloromethyl)-benzaldehyde is employed as an intermediate in the production of dyes. 3-(Chloromethyl)-benzaldehyde's structural features facilitate the synthesis of a range of dyes used in various applications, including textiles, plastics, and printing inks, due to its ability to undergo diverse chemical reactions.
It is crucial to handle 3-(Chloromethyl)-benzaldehyde with care due to the reactivity of the chloromethyl group, which can present health risks if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 77072-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,7 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77072-00:
(7*7)+(6*7)+(5*0)+(4*7)+(3*2)+(2*0)+(1*0)=125
125 % 10 = 5
So 77072-00-5 is a valid CAS Registry Number.
77072-00-5Relevant articles and documents
Modular synthesis of triazole-containing triaryl α-helix mimetics
Ehlers, Ina,Maity, Prantik,Aube, Jeffrey,Koenig, Burkhard
scheme or table, p. 2474 - 2490 (2011/06/10)
We describe novel scaffold designs for nonpeptidic α-helix mimetics. The tricyclic scaffolds contain triazoles and reproduce amino acid side chains i, i+3, and i+7. The three different scaffolds are synthetically readily accessible, allow the introduction
