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5H-Pyrrolo(2,1-c)(1,4)benzodiazepin-5-one, 1,2,3,10,11,11a-hexahydro- is a complex organic compound belonging to the class of benzodiazepines. This molecule is characterized by a pyrrolo fused to a benzodiazepine ring system, with six hydrogen atoms attached to the carbon atoms at positions 1, 2, 3, 10, 11, and 11a. The compound exhibits a hexahydro structure, indicating the presence of six hydrogen atoms bonded to carbon atoms in a cyclic manner. This specific chemical structure is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting the central nervous system. The compound's unique properties and structure make it a subject of interest for further exploration in medicinal chemistry.

5544-20-7

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5544-20-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5544-20-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,4 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5544-20:
(6*5)+(5*5)+(4*4)+(3*4)+(2*2)+(1*0)=87
87 % 10 = 7
So 5544-20-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2O/c15-12-10-5-1-2-6-11(10)13-8-9-4-3-7-14(9)12/h1-2,5-6,9,13H,3-4,7-8H2

5544-20-7SDS

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 5,6,6a,7,8,9-hexahydropyrrolo[2,1-c][1,4]benzodiazepin-11-one

1.2 Other means of identification

Product number -
Other names 5-Oxo-2,3,5,10,11,11a-hexahydro-1H-pyrrolo<benzdiazepin

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:5544-20-7 SDS

5544-20-7Downstream Products

5544-20-7Relevant academic research and scientific papers

Selective reduction of secondary amides to amines in the presence of tertiary amides

Lee, Byung H.,Clothier, Michael F.

, p. 643 - 644 (1999)

Secondary amides activated with a Cbz group can be reduced to their corresponding hemiaminals using lithium borohydride. Hydrogenation then removes the Cbz and hydroxyl groups to produce the related amine. Tertiary amides are not affected.

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