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3H-Diazirine, 3-chloro-3-(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29648-80-4

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29648-80-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29648-80-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,4 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29648-80:
(7*2)+(6*9)+(5*6)+(4*4)+(3*8)+(2*8)+(1*0)=154
154 % 10 = 4
So 29648-80-4 is a valid CAS Registry Number.

29648-80-4SDS

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 3-chloro-3-propan-2-yldiazirine

1.2 Other means of identification

Product number -
Other names 3-chloro-3-isopropyl-3H-diazirine

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:29648-80-4 SDS

29648-80-4Downstream Products

29648-80-4Relevant academic research and scientific papers

Competitive rearrangements of alkylacetoxycarbenes

Moss, Robert A.,Xue, Song,Ma, Wei,Ma, Huarong

, p. 4379 - 4382 (2007/10/03)

Absolute rate constants are determined for (1,2) acetyl, carbon, andhydride shifts in cyclobutylacetoxycarbene and isopropylacetoxycarbene; comparative reactivities are examined.

On the Mechanism of Graham's Reaction

Moss, Robert A.,Wlostowska, Joanna,Guo, Wenjeng,Fedorynski, Michal,Springer, James P.,Hirshfield, Jordan M.

, p. 5048 - 5050 (2007/10/02)

The oxidative cyclization of amidines to 3-chloro-3-substituted diazirines with aqueous sodium hypochlorite proceeds through N-chloro- and N,N'-dichloroamidines; the latter are isolable in certain cases.

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