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1H-1,4-Benzodiazepine-3-carboxylic acid, 2,3-dihydro-7-methyl-2-oxo-5-phenyl, ethyl ester is a complex organic compound belonging to the benzodiazepine class. This molecule features a benzodiazepine core structure, which is a fused ring system consisting of a diazepine (a seven-membered ring with two nitrogen atoms) and a benzene ring. The compound is characterized by a 2,3-dihydro-7-methyl-2-oxo-5-phenyl substitution pattern, indicating the presence of a methyl group at the 7-position, an oxygen atom at the 2-position, and a phenyl group at the 5-position. The ethyl ester functional group is attached to the carboxylic acid moiety, which is part of the benzodiazepine core. This chemical structure is significant in medicinal chemistry, as benzodiazepines are known for their anxiolytic, sedative, and anticonvulsant properties. The specific arrangement of substituents in 1H-1,4-Benzodiazepine-3-carboxylic acid, 2,3-dihydro-7-methyl-2-oxo-5-phenyl-, ethyl ester may influence its pharmacological activity and potential therapeutic applications.

5571-87-9

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5571-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5571-87-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,7 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5571-87:
(6*5)+(5*5)+(4*7)+(3*1)+(2*8)+(1*7)=109
109 % 10 = 9
So 5571-87-9 is a valid CAS Registry Number.

5571-87-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepine-3-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 7-Methyl-3-ethoxycarbonyl-5-phenyl-2-oxo-2,3-dihydro-1H-benzo[f]-1,4-diazepine

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:5571-87-9 SDS

5571-87-9Upstream product

5571-87-9Downstream Products

5571-87-9Relevant 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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