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1,3-diazepane-2,5-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72331-38-5

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72331-38-5 Usage

Type of compound

Heterocyclic compound

Definition of heterocyclic compound

A compound with a ring structure that includes at least two different elements

Usage

Building block in the synthesis of pharmaceuticals and in organic chemistry research

Potential applications

Medicinal chemistry

Reason for potential applications

Ability to bind to various biological targets and diverse pharmacological activities

Importance

Structure and reactivity make it an important intermediate in the development of new drugs and therapeutic agents

Check Digit Verification of cas no

The CAS Registry Mumber 72331-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,3 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72331-38:
(7*7)+(6*2)+(5*3)+(4*3)+(3*1)+(2*3)+(1*8)=105
105 % 10 = 5
So 72331-38-5 is a valid CAS Registry Number.

72331-38-5SDS

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 1,3-diazepane-2,5-dione

1.2 Other means of identification

Product number -
Other names perhydro-1,3-diazepin-2,5-dione

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:72331-38-5 SDS

72331-38-5Relevant academic research and scientific papers

Seven-membered ring compounds as inhibitors of cytidine deaminase

-

, (2008/06/13)

Seven-membered heterocyclic nucleosides used to inhibit the deamination enzyme responsible for the inactivation of arabinosylcytosine (ara--C). Preferred nucleosides containing a seven-member aglycone are as follows: STR1 Preferred aglycones are as follow

1,3-Diazepinones. 1. Synthesis of 5-Hydroxyperhydro-1,3-diazepin-2-one

Marquez, Victor E.,Liu, Paul S.,Kelley, James A.,Driscoll, John S.

, p. 485 - 489 (2007/10/02)

The synthesis of 5-hydroxyperhydro-1,3-diazepin-2-one (3) is accomplished by two different routes.The first route involves the reduction of the precursor ketone 2, which is synthesized in seven steps from levulinic acid (5).The second approach makes use of the hydration of the symmetrically unsaturated precursor 4 via the hydroboration-oxidation procedure.This precursor in turn is obtained by direct cyclization of cis-1,4-diamino-2-butene (12).

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