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3-Azetidinol, 1-(phenylmethyl)-, hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

223382-13-6

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223382-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 223382-13-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,3,8 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 223382-13:
(8*2)+(7*2)+(6*3)+(5*3)+(4*8)+(3*2)+(2*1)+(1*3)=106
106 % 10 = 6
So 223382-13-6 is a valid CAS Registry Number.

223382-13-6SDS

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 1-Benzyl-3-hydroxyazetidinium chloride

1.2 Other means of identification

Product number -
Other names 1-benzylazetidine-3-ol hydrochloride

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:223382-13-6 SDS

223382-13-6Relevant academic research and scientific papers

Development of an optimized process for the preparation of 1-benzylazetidin-3-ol: An industrially important intermediate for substituted azetidine

Krishna Reddy,Udaykiran,Chintamani,Mahesh Reddy,Kameswararao, Ch.,Madhusudhan

, p. 462 - 466 (2012/01/17)

A thoroughly optimized and robust process for the synthesis of 1-benzylazetidin-3-ol has been emphasized. 1-Benzylazetidin-3-ol has been utilized as a starting material in the commercial synthesis of azetidin-3-ol hydrochloride. Synthesis of azetidin-3-ol hydrochloride involves the usage of very low cost and commercially available starting material (benzylamine) and with reduced formation of di(3-chloro-2-hydroxypropyl) benzylamine significantly resulting in an economical process that allows the effective production of 1-benzyl azetidin-3-ol as well as azetidin-3-ol hydrochloride.

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