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2210-07-3

Hexahydro-5-methyl-2H-azepin-2-one is a cyclic amine derivative with the molecular formula C7H13NO. It is a colorless to pale yellow liquid with a molecular weight of 127.19 g/mol. Hexahydro-5-methyl-2H-azepin-2-one is characterized by a seven-membered azepine ring, which includes a nitrogen atom, and a methyl group attached to the fifth carbon. The ketone functional group is present at the second position, indicating the presence of a carbonyl group (C=O). Hexahydro-5-methyl-2H-azepin-2-one is synthesized through various chemical reactions and is used as an intermediate in the preparation of pharmaceuticals and other organic compounds. It is important to handle this chemical with care due to its potential reactivity and toxicity.

2210-07-3

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2210-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2210-07-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2210-07:
(6*2)+(5*2)+(4*1)+(3*0)+(2*0)+(1*7)=33
33 % 10 = 3
So 2210-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO/c1-6-2-3-7(9)8-5-4-6/h6H,2-5H2,1H3,(H,8,9)

2210-07-3SDS

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-methylazepan-2-one

1.2 Other means of identification

Product number -
Other names 5-methyl-azepan-2-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:2210-07-3 SDS

2210-07-3Downstream Products

2210-07-3Relevant articles and documents

Silica sulfuric acid as a reusable catalyst for the conversion of ketones into amides by a Schmidt reaction under solvent-free conditions

Eshghi, Hossein,Hassankhani, Asadollah,Mosaddegh, Elaheh

, p. 218 - 219 (2007/10/03)

Silica sulfuric acid is a highly efficient reagent for the conversion of a variety of ketones into the corresponding amides by a Schmidt reaction under solvent-free conditions. Cyclic, aliphatic and aromatic ketones with electron-donating or withdrawing substituents may be converted easily in excellent yield. The major advantages of this method are: operational simplicity, the ready availability of the reagent, selectivity, general applicability, mild reaction conditions, short reaction times and high yields. The recovered catalyst could be used in new attempts without any purification.

P2O5/SiO2-catalyzed one-pot synthesis of amides from ketones via schmidt reaction under microwave irradiation in dry media

Eshghi, Hossein,Hassankhani, Asadollah

, p. 2211 - 2216 (2007/10/03)

A facile and efficient method for the preparation of amides from ketones by the Schmidt reaction is described for the first time using P 2 O 5 /SiO 2 and sodium azide under solvent-free microwave irradiation. Advantages of this procedure are selectivity, good yields, a simple operation, short reaction time, and solvent-free conditions. Copyright Taylor & Francis Group, LLC.

Amidino derivatives useful as nitric oxide synthase inhibitors

-

, (2008/06/13)

The current invention discloses useful pharmaceutical compositions containing amidino derivative useful as nitric oxide synthase inhibitors.

2-Iminohomopiperidinium salts as selective inhibitors of inducible nitric oxide synthase (iNOS)

Hansen Jr., Donald W.,Peterson, Karen B.,Trivedi, Mahima,Kramer, Steven W.,Webber, Ronald K.,Tjoeng, Foe S.,Moore, William M.,Jerome, Gina M.,Kornmeier, Christine M.,Manning, Pamela T.,Connor, Jane R.,Misko, Thomas P.,Currie, Mark G.,Pitzele, Barnett S.

, p. 1361 - 1366 (2007/10/03)

An attractive approach to the treatment of inflammatory conditions such as osteo- and rheumatoid arthritis, inflammatory bowel disease, and sepsis is through the selective inhibition of human inducible nitric oxide synthase (hiNOS) since localized excess

Amidino dervatives useful as nitric oxide synthase inhibitors

-

, (2008/06/13)

The current invention discloses useful pharmaceutical compositions containing azepine derivatives useful as nitric oxide synthase inhibitors.

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