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36260-84-1

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36260-84-1 Usage

Structure

Substituted azetidine, a four-membered heterocycle ring containing nitrogen

Tert-butyl group

Attached to the first carbon atom of the azetidine ring (CH3)3C-

Usage

Building block in organic synthesis for the preparation of various pharmaceuticals, agrochemicals, and materials

Unique properties

Known for its unique steric and electronic properties, making it a valuable intermediate in the chemical industry

Potential applications

Studied for its potential applications in catalysts, polymers, and other advanced materials

Check Digit Verification of cas no

The CAS Registry Mumber 36260-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,6 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36260-84:
(7*3)+(6*6)+(5*2)+(4*6)+(3*0)+(2*8)+(1*4)=111
111 % 10 = 1
So 36260-84-1 is a valid CAS Registry Number.

36260-84-1SDS

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 1-tert-butylazetidine

1.2 Other means of identification

Product number -
Other names Azetidine,1-(1,1-dimethylethyl)

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:36260-84-1 SDS

36260-84-1Downstream Products

36260-84-1Relevant articles and documents

Microwave-assisted synthesis of azetidines in aqueous media

Burkett, Brendan A.,Ting, Samuel Z.,Gan, Gwendolyn C. S.,Chai, Christina L. L.

supporting information; experimental part, p. 6590 - 6592 (2011/02/23)

Simple azetidines are synthesized in good to excellent yields and high purity via cyclization of 3-(ammo-nio)propyl sulfates derived from primary amines and the cyclic sulfate of 1,3-propanediol. A feature of this methodology includes the accelerated synt

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