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142835-68-5

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142835-68-5 Usage

Molecular Weight

129.16 g/mol

Physical Appearance

Colorless to pale yellow liquid

Functional Group

Aziridinecarboxylic acid

Configuration

Trans-configuration

Main Use

Building block in organic synthesis and pharmaceutical production

Properties

Trans-configuration: Imparts specific chemical and pharmacological properties
Reactivity: Potential applications in medicinal chemistry and drug discovery

Potential Applications

Medicinal chemistry
Drug discovery

Check Digit Verification of cas no

The CAS Registry Mumber 142835-68-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,8,3 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 142835-68:
(8*1)+(7*4)+(6*2)+(5*8)+(4*3)+(3*5)+(2*6)+(1*8)=135
135 % 10 = 5
So 142835-68-5 is a valid CAS Registry Number.

142835-68-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Aziridinecarboxylicacid,1-methoxy-3-methyl-,methylester,trans-(9CI)

1.2 Other means of identification

Product number -
Other names -

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:142835-68-5 SDS

142835-68-5Downstream Products

142835-68-5Relevant articles and documents

Synthesis of N-Methoxy and N-H Aziridines from Alkenes

Vedejs, Edwin,Sano, Hiroshi

, p. 3261 - 3264 (2010/11/30)

Electron-rich alkenes are converted into N-methoxyaziridines by treatment with HN(OCH3)2 and trimethylsilyl triflate.Reduction with Li/ammonia affords the N-H aziridines. Key words: Aziridine; N-methoxyaziridine; N-methoxycaprolactam; dimethoxyamine; nitrenium ion

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