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21635-88-1

21635-88-1

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21635-88-1 Usage

Chemical Properties

Colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 21635-88-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,3 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21635-88:
(7*2)+(6*1)+(5*6)+(4*3)+(3*5)+(2*8)+(1*8)=101
101 % 10 = 1
So 21635-88-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H7NO/c4-3-1-5-2-3/h3H,1-2,4H2

21635-88-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail

  • Alfa Aesar

  • (H57248)  3-Aminooxetane, 95%   

  • 21635-88-1

  • 250mg

  • 1764.0CNY

  • Detail

  • Alfa Aesar

  • (H57248)  3-Aminooxetane, 95%   

  • 21635-88-1

  • 500mg

  • 2940.0CNY

  • Detail

  • Aldrich

  • (777838)  3-Aminooxetane  97%

  • 21635-88-1

  • 777838-500MG

  • 1,248.39CNY

  • Detail

21635-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name oxetan-3-amine

1.2 Other means of identification

Product number -
Other names 3-Oxetanamin

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:21635-88-1 SDS

21635-88-1Upstream product

21635-88-1Relevant articles and documents

Synthesis of Electron-Deficient Oxetanes. 3-Azidooxetane, 3-Nitrooxetane, and 3,3-Dinitrooxetane

Baum, Kurt,Berkowitz, Phillip T.,Grakauskas, Vytautas,Archibald, Thomas G.

, p. 2953 - 2956 (2007/10/02)

A facile synthesis of 3-hydroxyoxetane is described and is based on the addition of acetic acid to epichlorohydrin, protection of the resulting primary alcohol as an acetal, basic acetate hydrolysis and ring closure, and removal of the protecting group. 3-Azidooxetane was prepared from 3-(tosyloxy)oxetane and sodium azide.Reduction of the azide with triphenylphosphine or hydrogen gave 3-aminooxetane, and oxidation of the amine with m-chloroperbenzoic acid gave 3-nitrooxetane.Oxidative nitration or reaction with tetranitromethane gave 3,3-dinitrooxetane. 3-Azidooxetane and 3,3-dinitrooxetane were polymerized with Lewis acids.

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