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5-(4-chlorophenyl)-1,3,5-dithiazinane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93282-07-6

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93282-07-6 Usage

Chemical compound

5-(4-chlorophenyl)-1,3,5-dithiazinane

Class of compounds

Dithiazinane

Ring system

1,3,5-dithiazinane

Substituent

4-chlorophenyl

Usage

Organic chemistry, potential pharmaceutical or industrial applications
Versatile building block for synthesizing complex compounds

Check Digit Verification of cas no

The CAS Registry Mumber 93282-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,8 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93282-07:
(7*9)+(6*3)+(5*2)+(4*8)+(3*2)+(2*0)+(1*7)=136
136 % 10 = 6
So 93282-07-6 is a valid CAS Registry Number.

93282-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-chlorophenyl)-1,3,5-dithiazinane

1.2 Other means of identification

Product number -
Other names -

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:93282-07-6 SDS

93282-07-6Downstream Products

93282-07-6Relevant academic research and scientific papers

Synthesis of Thiocarbonyl and Heterocyclic Compounds from 2-Methylene-1,3-dithietanes

Okajima, Nobuyuki,Okada, Yoshiyuki

, p. 567 - 574 (2007/10/02)

2-Methyl-1,3-dithietanes bearing electron withdrawing groups on the methylene carbon atom were synthesized and their reactivities were studied.These compounds readily underwent a ring-opening reaction with a variety of nucleophilic reagents such as amines

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