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1H-1,4-Benzodiazepine, 2,3-dihydro-5-phenyl- is a chemical compound belonging to the benzodiazepine class, which is characterized by a fused benzene ring and a diazepine ring. This specific compound features a phenyl group attached to the 5th position of the diazepine ring, and it has a 2,3-dihydro structure, indicating the presence of two hydrogen atoms in the 2nd and 3rd positions, which are part of a saturated ring. Benzodiazepines are known for their various applications, particularly in the pharmaceutical industry, where they are used as sedatives, hypnotics, and anticonvulsants. The 2,3-dihydro-5-phenyl derivative may exhibit different pharmacological properties compared to other benzodiazepines due to its unique structural features.

2898-20-6

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2898-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2898-20-6 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 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2898-20:
(6*2)+(5*8)+(4*9)+(3*8)+(2*2)+(1*0)=116
116 % 10 = 6
So 2898-20-6 is a valid CAS Registry Number.

2898-20-6SDS

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-2,3-dihydro-1H-1,4-benzodiazepine

1.2 Other means of identification

Product number -
Other names 1H-1,4-Benzodiazepine,2,3-dihydro-5-phenyl

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:2898-20-6 SDS

2898-20-6Relevant academic research and scientific papers

Design, synthesisand preliminary evaluation of a series of histone deacetylase inhibitors carrying a benzodiazepine ring

Guandalini,Balliu,Cellai,Martino,Nebbioso,Mercurio,Carafa,Bartolucci,Dei,Manetti,Teodori,Scapecchi,Altucci,Paoletti,Romanelli

, p. 56 - 68 (2013/10/01)

A series of new histone deacetylase inhibitors were designed and synthesized based on hybridization between SAHA or oxamflatin and 5-phenyl-1,4-benzodiazepines. The compounds were tested for their enzyme inhibitory activity on HeLa nuclear extracts, and o

CHEMICAL COMPOUNDS

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Page/Page column 50, (2008/06/13)

The present invention relates to dihydrobenzodiazepine derivatives, compositions and medicaments containing the same, as well as processes for the preparation and use of such compounds, compositions and medicaments. Such dihydrobenzodiazepine derivatives

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