38076-67-4 Usage
General Description
Phenothiazine-10-carboxaldehyde is a chemical compound that belongs to the phenothiazine class of organic compounds. It is widely used in the pharmaceutical industry for its antibacterial and antifungal properties, as well as its potential use as a building block in the synthesis of other compounds. Phenothiazine-10-carboxaldehyde has been studied for its antiproliferative and anti-inflammatory activities, making it a promising candidate for drug development. Its unique chemical structure and diverse properties make it a valuable tool for researchers in various scientific fields.
Check Digit Verification of cas no
The CAS Registry Mumber 38076-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,7 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 38076-67:
(7*3)+(6*8)+(5*0)+(4*7)+(3*6)+(2*6)+(1*7)=134
134 % 10 = 4
So 38076-67-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H9NOS/c15-9-14-10-5-1-3-7-12(10)16-13-8-4-2-6-11(13)14/h1-9H
38076-67-4Relevant articles and documents
The singlet oxygen oxidation of chlorpromazine and some phenothiazine derivatives. Products and reaction mechanisms
Baciocchi, Enrico,Del Giacco, Tiziana,Lanzalunga, Osvaldo,Lapi, Andrea,Raponi, Daniele
, p. 5912 - 5915 (2008/02/10)
(Chemical Equation Presented) A kinetic and product study of the reactions of chlorpromazine 1, N-methylphenothiazine 2, and N-ethylphenothiazine 3 with singlet oxygen was carried out in MeOH and MeCN. 1 undergoes exclusive side-chain cleavage, whereas the reactions of 2 and 3, in MeOH, afforded only the corresponding sulfoxides. A mechanism for the reaction of 1 is proposed where the first step involves an interaction between singlet oxygen and the side-chain dimethylamino nitrogen. This explains why no side-chain cleavage is observed for 2 and 3.