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5441-40-7

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5441-40-7 Usage

General Description

2,5-Diaza-5-methylcycloheptanone is a chemical compound with the molecular formula C7H13NO. It is a cyclic ketone with a seven-membered ring containing two nitrogen atoms. 2,5-Diaza-5-methylcycloheptanone is used as a building block in organic synthesis and can undergo various reactions to form different derivatives. It is also known for its potential application as a ligand in coordination chemistry, particularly in the formation of metal complexes. The chemical properties and reactivity of 2,5-Diaza-5-methylcycloheptanone make it a valuable component in the development of pharmaceuticals and other fine chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 5441-40-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5441-40:
(6*5)+(5*4)+(4*4)+(3*1)+(2*4)+(1*0)=77
77 % 10 = 7
So 5441-40-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N2O/c1-8-4-2-6(9)7-3-5-8/h2-5H2,1H3,(H,7,9)

5441-40-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methyl-1,4-diazepan-5-one

1.2 Other means of identification

Product number -
Other names 1-methyl-1,4-diazepan-5-one

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:5441-40-7 SDS

5441-40-7Relevant articles and documents

Selective heterocyclic amidine inhibitors of human inducible nitric oxide synthase

Moormann, Alan E.,Metz, Sue,Toth, Mihaly V.,Moore, William M.,Jerome, Gina,Kornmeier, Christine,Manning, Pamela,Hansen Jr., Donald W.,Pitzele, Barnett S.,Webber

, p. 2651 - 2653 (2007/10/03)

The potency and selectivity of a series of 5-hetero-2-iminohexahydroazepines were examined as inhibitors of the three human NOS isoforms. The effect of ring substitution of the 5-carbon for a heteroatom is presented. Potencies (IC50's) for these inhibitors are in the low micromolar range for hi-NOS with some examples exhibiting a 500× selectivity versus hec-NOS.

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