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5-(2-fluorophenyl)-7-iodo-1,3-dihydro-2H-1,4-benzodiazepin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30843-56-2

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30843-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30843-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,4 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30843-56:
(7*3)+(6*0)+(5*8)+(4*4)+(3*3)+(2*5)+(1*6)=102
102 % 10 = 2
So 30843-56-2 is a valid CAS Registry Number.

30843-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(2-fluorophenyl)-7-iodo-1,3-dihydro-1,4-benzodiazepin-2-one

1.2 Other means of identification

Product number -
Other names Ro 7-9749

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:30843-56-2 SDS

30843-56-2Downstream Products

30843-56-2Relevant academic research and scientific papers

Triazolobenzo- and triazolothienodiazepines as potent antagonists of platelet activating factor

Walser,Flynn,Mason,Crowley,Maresca,Yaremko,O'Donnell

, p. 1209 - 1221 (2007/10/02)

A series of [1,2,4]triazolo[4,3-α][1,4]benzodiazepines bearing an ethynyl functionality at the 8-position and the isosteric thieno[3,2-f][1,2,4]triazolo[4,3-α][1,4]diazepines were prepared and evaluated as antagonists of platelet activating factor. The effects of substitution were explored in in vitro and in vivo test systems designed to measured PAF-antagonistic activity. Results are discussed and compared with previously published data. Many of the compounds had activity superior to WEB 2086, compound 1. In general, the thieno analogues exhibited better oral activity than the corresponding benzodiazepines. The duration of activity upon oral administration was modulated by the substitution on the acetylenic side chain. Compounds 71 and 81 were selected for further pharmacological evaluation as a result of their good oral potency and exceptionally long duration of action.

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