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2,3-Dihydro-5-phenyl-7-(trifluoromethyl)-1H-1,4-benzodiazepine is a complex organic compound belonging to the benzodiazepine class. It is characterized by a dihydrobenzodiazepine ring structure, with a phenyl group at the 5th position and a trifluoromethyl group at the 7th position. 2,3-Dihydro-5-phenyl-7-(trifluoromethyl)-1H-1,4-benzodiazepine is known for its potential pharmacological properties, particularly as a sedative, anxiolytic, and anticonvulsant agent. Its chemical structure contributes to its ability to interact with the GABA receptor, which plays a crucial role in the central nervous system's inhibitory processes. The trifluoromethyl group adds a unique characteristic to the molecule, potentially affecting its lipophilicity and metabolic stability. While it shares some properties with other benzodiazepines, the specific arrangement of functional groups in 2,3-Dihydro-5-phenyl-7-(trifluoromethyl)-1H-1,4-benzodiazepine may confer distinct therapeutic benefits and side effect profiles.

2890-28-0

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2890-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2890-28-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2890-28:
(6*2)+(5*8)+(4*9)+(3*0)+(2*2)+(1*8)=100
100 % 10 = 0
So 2890-28-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H13F3N2/c17-16(18,19)12-6-7-14-13(10-12)15(21-9-8-20-14)11-4-2-1-3-5-11/h1-7,10,20H,8-9H2

2890-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenyl-7-(trifluoromethyl)-2,3-dihydro-1H-1,4-benzodiazepine

1.2 Other means of identification

Product number -
Other names 2,3-Dihydro-5-phenyl-7-trifluormethyl-1H-1,4-benzodiazepin

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:2890-28-0 SDS

2890-28-0Upstream product

2890-28-0Downstream Products

2890-28-0Relevant academic research and scientific papers

Process for preparing 1,4-benzodiazepines

-

, (2008/06/13)

1,4-Benzodiazepine derivatives of the formula, STR1 wherein R1 is hydrogen, a lower alkyl, a haloalkyl, a cycloalkylalkyl, an alkoxyalkyl, an acyloxyalkyl, an alkylthioalkyl, an alkylaminoalkyl, a dialkylaminoalkyl, a hydroxyalkyl, carbamoyl, or an N-alkylcarbamoyl; R2 is hydrogen or a lower alkyl; X is hydrogen, a halogen, nitro, or trifluoromethyl; A is a group of the formula, STR2 (wherein Y and Z each represent hydrogen, a halogen, a lower alkyl, or nitro) and a salt thereof, are prepared by reacting a 1,4-benzodiazepin-2-one compound of the formula, STR3 wherein R1, R2, X, Y and Z are the same as defined above, with diborane in an inert solvent.

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