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38076-73-2

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38076-73-2 Usage

Class of compounds

Phenothiazine

Type of compound

Derivative of phenothiazine

Therapeutic properties

Antipsychotic and antiemetic agent

Applications

Treatment of mental disorders (schizophrenia, bipolar disorder)

Potential

Anti-cancer agent (some studies)

Receptor affinity

High affinity for dopamine receptors in the brain

Role

Instrumental in the development of various psychoactive medications

Interest

Fields of medicine and pharmaceutical research

Unique features

Structure and properties that make it a subject of ongoing study and development

Check Digit Verification of cas no

The CAS Registry Mumber 38076-73-2 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, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38076-73:
(7*3)+(6*8)+(5*0)+(4*7)+(3*6)+(2*7)+(1*3)=132
132 % 10 = 2
So 38076-73-2 is a valid CAS Registry Number.

38076-73-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name phenothiazin-10-yl(phenyl)methanone

1.2 Other means of identification

Product number -
Other names 10-benzoyl-10H-phenothiazine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:38076-73-2 SDS

38076-73-2Relevant articles and documents

Utilizing d–pπ Bonds for Ultralong Organic Phosphorescence

Tian, Shuai,Ma, Huili,Wang, Xuan,Lv, Anqi,Shi, Huifang,Geng, Yun,Li, Jie,Liang, Fushun,Su, Zhong-Min,An, Zhongfu,Huang, Wei

supporting information, p. 6645 - 6649 (2019/04/04)

Developing pure organic materials with ultralong lifetimes is attractive but challenging. Here we report a concise chemical approach to regulate the electronic configuration for phosphorescence enhancement. After the introduction of d–pπ bonds into a phenothiazine model system, a phosphorescence lifetime enhancement of up to 19 times was observed for DOPPMO, compared to the reference PPMO. A record phosphorescence lifetime of up to 876 ms was obtained in phosphorescent phenothiazine. Theoretical calculations and single-crystal analysis reveal that the d–pπ bond not only reduces the (n, π*) proportion of the T1 state, but also endows the rigid molecular environment with multiple intermolecular interactions, thus enabling long-lived phosphorescence. This finding makes a valuable contribution to the prolongation of phosphorescence lifetimes and the extension of the scope of phosphorescent materials.

Synthesis and bio-evaluation of phenothiazine derivatives as new anti-tuberculosis agents

He, Chun-Xian,Meng, Hui,Zhang, Xiang,Cui, Hua-Qing,Yin, Da-Li

supporting information, p. 951 - 954 (2015/08/18)

Abstract Two series of phenothiazine derivatives were designed and synthesized. All compounds were tested for anti-tuberculosis activities against Mycobacterium tuberculosis H37RV. In comparison with mother compound of chlorpromazine, compound 6e shows promising anti-tuberculosis activity and much less mammalian cell cytotoxicity, compound 6e merits to be further explored as new anti-tuberculosis agents.

N-benzoylated phenoxazines and phenothiazines: Synthesis, antiproliferative activity, and inhibition of tubulin polymerization

Prinz, Helge,Chamasmani, Behfar,Vogel, Kirsten,B?hm, Konrad J.,Aicher, Babette,Gerlach, Matthias,Günther, Eckhard G.,Amon, Peter,Ivanov, Igor,Müller, Klaus

supporting information; experimental part, p. 4247 - 4263 (2011/08/05)

A total of 53 N-benzoylated phenoxazines and phenothiazines, including their S-oxidized analogues, were synthesized and evaluated for antiproliferative activity, interaction with tubulin, and cell cycle effects. Potent inhibitors of multiple cancer cell l

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