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3-tert-Butyldiazirine is a chemical compound with the molecular formula C4H8N2. It is a cyclic diazirine derivative, characterized by a three-membered ring containing two nitrogen atoms and one carbon atom. 3-tert-Butyldiazirine is known for its high reactivity due to the strained nature of the diazirine ring, which makes it a valuable intermediate in organic synthesis. It can be used to generate carbenes, which are important in various chemical transformations. 3-tert-Butyldiazirine is also notable for its potential applications in the synthesis of pharmaceuticals and other specialty chemicals. However, due to its reactivity, it requires careful handling and is typically used in controlled laboratory settings.

1630-93-9

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1630-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1630-93-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,3 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1630-93:
(6*1)+(5*6)+(4*3)+(3*0)+(2*9)+(1*3)=69
69 % 10 = 9
So 1630-93-9 is a valid CAS Registry Number.

1630-93-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-tert-butyl-3H-diazirine

1.2 Other means of identification

Product number -
Other names t-Butyl-diazirin

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:1630-93-9 SDS

1630-93-9Upstream product

1630-93-9Downstream Products

1630-93-9Relevant academic research and scientific papers

A facile one-pot conversion of non-enolizable aldehydes to diazirines

Likhotvorik, Igor R.,Tae, Eunju Lee,Ventre, Celine,Platz, Matthew S.

, p. 795 - 796 (2000)

A general route to monoalkyl diazirines from non-enolizable aldehydes through N-trimethylsilyl diaziridines is described. (C) 2000 Elsevier Science Ltd.

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