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2H-1,4-Benzodiazepin-2-one, 7-chloro-1,3-dihydro-5-[2-(methylthio)phenyl]- is a complex organic compound belonging to the benzodiazepine class. This molecule is characterized by a benzodiazepine core, which is a fused ring system consisting of a diazepine ring and a benzene ring. The compound features a 7-chloro substitution, indicating the presence of a chlorine atom at the 7th position of the benzodiazepine ring. Additionally, it has a 1,3-dihydro group, which implies the presence of two hydrogen atoms attached to the first and third carbon atoms of the benzodiazepine ring, making it partially saturated. The molecule also contains a 2-(methylthio)phenyl group, which is a phenyl ring with a methylthio substituent at the 2nd position. 2H-1,4-Benzodiazepin-2-one, 7-chloro-1,3-dihydro-5-[2-(methylthio)phenyl]- is known for its potential pharmacological properties and is often studied for its therapeutic applications, particularly in the development of drugs targeting the central nervous system.

846-53-7

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846-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 846-53-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 846-53:
(5*8)+(4*4)+(3*6)+(2*5)+(1*3)=87
87 % 10 = 7
So 846-53-7 is a valid CAS Registry Number.

846-53-7SDS

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 7-chloro-5-(2-methylthiophenyl)-1,3-dihydro-1,4-benzodiazepin-2-one

1.2 Other means of identification

Product number -
Other names 7-chloro-5-(2-methylsulfanyl-phenyl)-1,3-dihydro-benzo[e][1,4]diazepin-2-one

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

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More Details:846-53-7 SDS

846-53-7Relevant academic research and scientific papers

REACTION OF 4-CHLORO-1-NITROBENZENE WITH o-SUBSTITUTED PHENYLACETONITRILES; SYNTHESIS OF 8-CHLORO-1-METHYL(AND METHYLTHIOMETHYL)-6-(2-SUBSTITUTED PHENYL)-4H-s-TRIAZOLO-1,4-BENZODIAZEPINES

Vejdelek, Zdenek,Holubek, Jiri,Ryska, Miroslav,Koruna, Ivan,Svatek, Emil,et.al.

, p. 2545 - 2563 (2007/10/02)

Reactions of 4-chloro-1-nitrobenzene with 2-methyl-, 2-methoxy- and 2-(methylthio)phenylacetonitrile in methanolic potassium hydroxide gave mixture from which the excepted 3-aryl-5-chloro-2,1-benzisoxazoles Ia-c were isolated in addition to the 2H-indoles IIIa and IIIc and acridines VIII and IX.The 2,1-benzisoxazoles were reduced to the 2-aminobenzophenones XIIa-c which were transformed via the phthalimidoacetamido compounds XIIIa-c to 5-aryl-7-chloro-1,3-dihydro-1,4-benzodiazepine-2-ones XVa-c.Treatment with phosphorus pentasulfide led to the thiones XVIa-c which reacted in boiling butanol either with acetohydrazide or with (methylthio)acetohydrazide to give the title compounds XVIIa-c and XVIIIa-c.They showed only weak anticonvulsant, incoordinating and central depressant effects.

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