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3-(2-Trifluoromethyl-10H-phenothiazin-10-yl)propiononitrile is a complex organic chemical compound with the molecular formula C16H12F3N3S. It is a derivative of phenothiazine, a heterocyclic compound with a tricyclic structure consisting of two benzene rings and a thiazine ring. The compound features a trifluoromethyl group (-CF3) at the 2-position of the phenothiazine ring, a propiononitrile group (-CH2CH2CN) at the 3-position, and a nitrile group (-CN) at the end of the propiononitrile chain. 3-(2-Trifluoromethyl-10H-phenothiazin-10-yl)propiononitrile is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of various drugs and agrochemicals. Its unique structure and properties make it a valuable compound for research and development in the field of medicinal chemistry.

573-14-8

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573-14-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 573-14-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 573-14:
(5*5)+(4*7)+(3*3)+(2*1)+(1*4)=68
68 % 10 = 8
So 573-14-8 is a valid CAS Registry Number.

573-14-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[2-(trifluoromethyl)phenothiazin-10-yl]propanenitrile

1.2 Other means of identification

Product number -
Other names HMS643G08

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:573-14-8 SDS

573-14-8Relevant academic research and scientific papers

Design, synthesis, and evaluation of efflux substrate-metal chelator conjugates as potential antimicrobial agents

Zhang, Yanling,Eric Ballard,Zheng, Shi-Long,Gao, Xingming,Ko, Ko-Chun,Yang, Hsiuchin,Brandt, Gary,Lou, Xinhui,Tai, Phang C.,Lu, Chung-Dar,Wang, Binghe

, p. 707 - 711 (2008/09/21)

Maintaining a proper balance of metal concentrations is critical to the survival of bacteria. We have designed and synthesized a series of conjugates of metal chelators and efflux transporter substrates aimed at disrupting bacterial metal homeostasis to a

Synthesis of phenothiazine derivatives as potential inhibitors of phospholipase C

Brufani,Cesta,Filocamo,Lappa,Marta,Pomponi,Meroni,Pagella

, p. 585 - 597 (2007/10/02)

In order to study the structure-activity relationships of phenothiazine derivatives inhibiting phosphatidylinositol-specific phospholipase C (PI-PLC), the synthesis of some phenothiazine amide, amine and ester derivatives was performed mainly by reacting 10H-phenothiazine-10-propanoyl chloride with some amines and alcohols; the resulting amides were reduced with borane to yield the corresponding amines. Starting from 2-chloro and 2-trifuoromethyl-10H-phenothiazine-10-propanoyl chloride two amides were synthesized. The inhibiting activity on PI-PLC from human platelets is reported.

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