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1H-1,2-Diazepine-1-carboxylicacid,methylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135360-85-9

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135360-85-9 Usage

Type of compound

Carboxylic acid ester derivative of 1H-1,2-diazepine (a seven-membered heterocyclic compound containing two nitrogen atoms)

Usage

Pharmaceutical and medicinal chemistry (synthesis of various drugs and bioactive molecules)

Biological activities

Antimicrobial, antifungal, and anticonvulsant properties

Potential applications

Development of new drug candidates for various therapeutic purposes

Significance

Plays a significant role in the advancement of drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 135360-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,3,6 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 135360-85:
(8*1)+(7*3)+(6*5)+(5*3)+(4*6)+(3*0)+(2*8)+(1*5)=119
119 % 10 = 9
So 135360-85-9 is a valid CAS Registry Number.

135360-85-9SDS

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 methyl diazepine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1H-1,2-DIAZEPINE-1-CARBOXYLIC ACID METHYL ESTER

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:135360-85-9 SDS

135360-85-9Relevant academic research and scientific papers

Asymmetric Synthesis of Diazepino-β-lactams by Cycloaddition of an 'Evans-Sjogren' Ketene with 1H-1,2-Diazepines

Muller, Marc,Bur, Daniel,Tschamber, Theophile,Streith, Jacques

, p. 767 - 773 (2007/10/02)

The ketene derivative of the chiral oxazolidone 1 underwent non-converted stereospecific cycloadditions with the (Z)-imine moiety of diazepines 2, leading thereby with good diastereoselection to the trans-β-lactam adducts 3 (major) and 4 (minor).T

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