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7-chloro-N-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepine-3-carboxamide is a complex organic compound belonging to the benzodiazepine class. It is characterized by a 1,4-benzodiazepine core structure, with a 7-chloro substitution, a methyl group attached to the nitrogen atom, and a phenyl group at the 5-position. The compound features a 2-oxo group, indicating the presence of a carbonyl group, and a 2,3-dihydro moiety, which implies the presence of two hydrogen atoms in the 2,3 positions of the benzodiazepine ring. This molecule is known for its potential pharmacological properties, particularly as a tranquilizer or sedative, due to its ability to interact with the GABA receptor in the central nervous system. However, it is important to note that the specific effects and safety profile of 7-chloro-N-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepine-3-carboxamide would need to be determined through rigorous scientific research and clinical trials.

5606-59-7

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5606-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5606-59-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,0 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5606-59:
(6*5)+(5*6)+(4*0)+(3*6)+(2*5)+(1*9)=97
97 % 10 = 7
So 5606-59-7 is a valid CAS Registry Number.

5606-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-chloro-N-methyl-2-oxo-5-phenyl-1,3-dihydro-1,4-benzodiazepine-3-carboxamide

1.2 Other means of identification

Product number -
Other names 7-Chloro-2,3-dihydro-N-methyl-2-oxo-5-phenyl-1H-1,4-benzodiazepine-3-carboxamide

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:5606-59-7 SDS

5606-59-7Upstream product

5606-59-7Downstream Products

5606-59-7Relevant academic research and scientific papers

Intermediates for preparing 1,4-benzodiazepine-2-ones having a carboxylic acid ester or amide group in the 3-position

-

, (2008/06/13)

Intermediates for preparing novel benzodiazepines having the formula SPC1 In which R1 is a hydrogen or halogen atom or a trifluoromethyl, loweralkyl, loweralkoxy, nitro or amino group; R2 is a furyl, a thienyl, cyclohexyl, a loweralkyl group or a phenyl group which may be substituted by a halogen atom or by a trifluoromethyl, nitro, loweralkoxy or loweralkyl group; and R3 is a hydrogen atom or a loweralkyl group; and R4 is lowercarbalkoxy, carbamoyl, N-loweralkylcarbamoyl, N,N-diloweralkylcarbamoyl, N-(diloweralkylaminoalkyl)carbamoyl, a group having the formula --COOCat in which Cat is a cation of an alkali metal or a semication of an alkaline earth metal or COOCat.CatOH, said intermediates being ortho-aminoaryl ketimines having the formula SPC2 Wherein R is hydrogen or EQU1 R1, R2, and R3 are as defined above, R4 is a hydrogen atom, a lowercarbalkoxy, carbamoyl, N-loweralkylcarbamoyl, N,N-diloweralkylcarbamoyl, N-(diloweralkylaminoalkyl)-carbamoyl, alkyl or substituted alkyl group; and R5 is a loweralkyl group.

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