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5-(2-fluorophenyl)-1-methyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one is a complex organic compound belonging to the benzodiazepine class. This molecule features a benzodiazepine core, which is a fused ring structure consisting of a diazepine ring (a seven-membered ring with two nitrogen atoms) and a benzene ring. The compound is characterized by the presence of a 2-fluorophenyl group (a phenyl ring with a fluorine atom at the 2-position) attached to the 5-position of the benzodiazepine core. Additionally, it has a methyl group at the 1-position and a ketone group at the 2-position. This chemical structure is significant in medicinal chemistry, as benzodiazepines are known for their anxiolytic, sedative, hypnotic, anticonvulsant, and muscle relaxant properties. The specific substitution patterns, such as the fluorine atom and the methyl group, can influence the pharmacological profile of the compound, potentially altering its potency, selectivity, and side effect profile.

844-11-1

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844-11-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 844-11-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 844-11:
(5*8)+(4*4)+(3*4)+(2*1)+(1*1)=71
71 % 10 = 1
So 844-11-1 is a valid CAS Registry Number.

844-11-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(2-fluorophenyl)-1-methyl-3H-1,4-benzodiazepin-2-one

1.2 Other means of identification

Product number -
Other names 1-Methyl-5-<2-fluor-phenyl>-1.3-dihydro-2H-1.4-benzodiazepin-2-on

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:844-11-1 SDS

844-11-1Downstream Products

844-11-1Relevant academic research and scientific papers

New synthesis of 1,3-dihydro-1,4-benzodiazepin-2(2H)-ones and 3-amino-1,3-dihydro-1,4-benzodiazepin-2(2H)-ones: Pd-catalyzed cross-coupling of imidoyl chlorides with organoboronic acids

Nadin, Alan,Sanchez Lopez, Jose M.,Owens, Andrew P.,Howells, Dean M.,Talbot, Adam C.,Harrison, Timothy

, p. 2844 - 2852 (2007/10/03)

A new approach to the synthesis of 1,4-benzodiazepines and 3-amino-1,4-benzodiazepines, which employs the Pd-catalyzed cross-coupling reaction of an imidoyl chloride with an organometallic reagent as the key step, is described. A five-step synthesis of a

Process for the preparation of 1,4-benzodiazepine derivatives

-

, (2008/06/13)

A 1,4-benzodiazepine derivative, or a pharmaceutically acceptable acid salt thereof, of the formula, SPC1 Wherein R1 is hydrogen, halogen, nitro or trifluoromethyl; R2 and R3 are independently hydrogen, halogen, lower alkyl or trifluoromethyl; R4 is lower alkyl, alkenyl, trihaloalkyl, alkoxyalkyl, alkenyloxyalkyl, alkoxyalkoxyalkyl, alkanoyloxyalkyl, cycloalkylalkyl, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl or a group of the formula EQU1 in which R6 and R7 are independently lower alkyl, and n is an integer of 1 to 4; and R5 is hydrogen or lower alkyl, is obtained by reacting a benzophenone derivative of the formula, SPC2 Wherein R1, R2, R3 and R4 are as defined above, with a 2-isocyanatoacetyl chloride derivative of the formula EQU2 wherein R5 is as defined above.

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