38076-67-4 Usage
Uses
Used in Pharmaceutical Industry:
Phenothiazine-10-carboxaldehyde is used as an active ingredient for its antibacterial and antifungal properties, contributing to the development of medications that combat various infections.
Used in Drug Development:
Phenothiazine-10-carboxaldehyde is used as a potential candidate for drug development due to its antiproliferative and anti-inflammatory activities, which can be harnessed to create new therapeutic agents for treating different health conditions.
Used in Chemical Synthesis:
Phenothiazine-10-carboxaldehyde is used as a building block in the synthesis of other compounds, allowing for the creation of a wide range of chemical products with various applications in different industries.
Used in Scientific Research:
Phenothiazine-10-carboxaldehyde is used as a valuable tool for researchers in various scientific fields, providing insights into its unique chemical structure and diverse properties, which can lead to new discoveries and advancements in related areas.
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 academic research and scientific papers
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.
