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37637-20-0

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37637-20-0 Usage

General Description

Azepan-2,5-dione, also known as 2,5-Diketohexahydro-1,4-epoxyazocine, is a chemical compound that belongs to the class of cyclic ketones. It has a six-membered ring structure with two carbonyl groups attached to it. AZEPAN-2,5-DIONE is primarily used as an intermediate in the production of pharmaceuticals and agrochemicals. It is also being studied for its potential use in organic chemical synthesis and as a building block for the synthesis of complex organic molecules. Azepan-2,5-dione has the potential to undergo various chemical reactions, making it a versatile compound with diverse applications in the field of chemistry and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 37637-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,3 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37637-20:
(7*3)+(6*7)+(5*6)+(4*3)+(3*7)+(2*2)+(1*0)=130
130 % 10 = 0
So 37637-20-0 is a valid CAS Registry Number.

37637-20-0SDS

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 2,5-Azepanedione

1.2 Other means of identification

Product number -
Other names Hexahydro-azepin-1-carbamid

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:37637-20-0 SDS

37637-20-0Relevant articles and documents

Kanaoka,Y.,Hatanaka,Y.

, p. 400 - 401 (1976)

Azido-Schmidt reaction for the formation of amides, imides and lactams from ketones in the presence of FeCl3

Yadav,Reddy, B.V. Subba,Reddy, U.V. Subba,Praneeth

, p. 4742 - 4745 (2008/12/21)

Ketones undergo smooth rearrangement with TMSN3 in the presence of FeCl3 under extremely mild conditions to provide the corresponding amides, imides and lactams in good yields with high selectivity. This method is very useful for the preparation of a wide range of amides, imides and lactams from ketones. The use of FeCl3 makes this method simple, convenient and cost-effective.

Central nervous system active compounds. X. some aspects of the photochemical rearrangement of N-alkylsuccinimides to hexahydroazepinones

Mooney,Prager,Ward

, p. 2695 - 2700 (2007/10/02)

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