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1H-1,4-Benzodiazepine-2,5-dione, 3,4-dihydro-1-methyl-4-phenyl- is a complex organic compound belonging to the benzodiazepine class. This molecule is characterized by a benzodiazepine core, which consists of a fused benzene ring and a diazepine ring. The compound features a 3,4-dihydro structure, indicating the presence of two hydrogen atoms attached to the carbon atoms at positions 3 and 4, which are part of a six-membered ring. Additionally, it has a methyl group (-CH3) at the 1-position and a phenyl group (C6H5) at the 4-position. This specific arrangement of functional groups and substituents gives the compound unique chemical and pharmacological properties, making it a potential candidate for various applications in the fields of medicine and chemistry.

1032-21-9

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1032-21-9 Usage

Chemical class

1H-1,4-Benzodiazepine-2,5-dione, 3,4-dihydro-1-methyl-4-phenylbelongs to the benzodiazepine class of drugs.

Sedative and anxiolytic properties

1H-1,4-Benzodiazepine-2,5-dione, 3,4-dihydro-1-methyl-4-phenyl- is known for its ability to induce sedation and reduce anxiety.

Derivative of 1,4-benzodiazepine

The compound is a derivative of the 1,4-benzodiazepine structure.

Methyl and phenyl group

It contains a methyl (CH3) and a phenyl (C6H5) group in its structure.

Central nervous system depressant

The compound is a potent central nervous system depressant.

Medical uses

It is used in the treatment of anxiety, insomnia, and seizures.

Potential for abuse and addiction

The compound is known for its potential to be abused and lead to addiction.

Mechanism of action

It acts on the GABA receptors in the brain, enhancing the inhibitory effects of the neurotransmitter GABA.

Sedative and calming effects

The enhancement of GABA's effects leads to the compound's sedative and calming properties.

Medical supervision

It is important to use this chemical under medical supervision due to its potential for addiction and adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 1032-21-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1032-21:
(6*1)+(5*0)+(4*3)+(3*2)+(2*2)+(1*1)=29
29 % 10 = 9
So 1032-21-9 is a valid CAS Registry Number.

1032-21-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-4-phenyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione

1.2 Other means of identification

Product number -
Other names 1-Methyl-4-phenyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione

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:1032-21-9 SDS

1032-21-9Downstream Products

1032-21-9Relevant academic research and scientific papers

Identification of the benzodiazepines as a new class of antileishmanial agent

Clark, Rachel L.,Carter, Katharine C.,Mullen, Alexander B.,Coxon, Geoffrey D.,Owusu-Dapaah, George,McFarlane, Emma,Duong Thi, M. Dao,Grant, M. Helen,Tettey, Justice N.A.,Mackay, Simon P.

, p. 624 - 627 (2007)

The continual increase in drug resistance; the lack of new chemotherapeutic agents; the toxicity of existing agents and the increasing morbidity with HIV co-infection mean the search for new antileishmanial agents has never been more urgent. We have ident

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