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

930-19-8

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930-19-8 Usage

Physical state

Colorless liquid.

Odor

Strong, ammonia-like.

Reactivity

Highly reactive.

Flammability

Flammable.

Primary use

As a monomer in the production of polymers and as a building block in organic synthesis.

Applications

Production of pharmaceuticals, agrochemicals, and other specialty chemicals.

Hazardous nature

Potential to cause skin and respiratory irritation, as well as environmental toxicity.

Safety precautions

Proper safety measures must be taken when handling and using 2,3-dimethylaziridine.

Check Digit Verification of cas no

The CAS Registry Mumber 930-19-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 930-19:
(5*9)+(4*3)+(3*0)+(2*1)+(1*9)=68
68 % 10 = 8
So 930-19-8 is a valid CAS Registry Number.

930-19-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-2,3-Dimethylaziridine

1.2 Other means of identification

Product number -
Other names cis-2,3-dimethyl-aziridine

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:930-19-8 SDS

930-19-8Relevant academic research and scientific papers

The Conversion of an Aziridine to a β-Lactam

Chamchaang, Wilaiporn,Pinhas, Allan R.

, p. 2943 - 2950 (2007/10/02)

A one-pot, inert atmosphere conversion of an aziridine to a β-lactam using nickel tetracarbonyl as the carbonyl source is described.In this reaction it is the less substituted carbon-nitrogen bond which is carbonylated.The proposed mechanism for this reac

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