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2,3,7,8-tetrachlorophenoxathiine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56348-76-6

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56348-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56348-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,4 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56348-76:
(7*5)+(6*6)+(5*3)+(4*4)+(3*8)+(2*7)+(1*6)=146
146 % 10 = 6
So 56348-76-6 is a valid CAS Registry Number.

56348-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,7,8-tetrachlorophenoxathiine

1.2 Other means of identification

Product number -
Other names 2,3,7,8-tetrachlorophenoxthin

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:56348-76-6 SDS

56348-76-6Upstream product

56348-76-6Downstream Products

56348-76-6Relevant academic research and scientific papers

The study on UV-degradation dynamics of 2,3,7,8-tetrachlorodibenzo-p-dioxin and its analogues

Qin, Zhaohai

, p. 91 - 97 (1996)

A study on UV-degradation dynamics of 2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3,7,8-TCDD) and its analogues 2,3,7,8-tetrachlorophenoxthin (2,3,7,8-TCPT) and 2,3,7,8-tetrachlorothianthrene (2,3,7,8-TCTR) in solvents CHCl3 and CCl4 was completed. The results indicated that they were degradated by UV in different way in different solvent. The degradation of 2,3,7,8-TCDD and 2,3,7,8-TCPT are pseudo-first-order reactions in CHCl3, but complex reactions in CCl4; the degradation of 2,3,7,8-TCTR is a zero-order reaction in CHCl3, but a pseudo-first-order reaction in CCl4. All of the three compounds disappeared in CCl4 much faster than in CHCl3 under 254 nm UV-irradiation.

Sulfuryl chloride in the synthesis of derivatives of dibenzothiophene, phenoxathiin, and thianthrene

Savin,Nedel'kin,Zverev

, p. 333 - 337 (2007/10/03)

Reactions of sulfuryl chloride with dibenzothiophene and related heterocyclic systems have been studied. It is shown that under different conditions, C- or S-halogenation of the heterocycle takes place. A series of new chlorine derivatives of dibenzothiophene, phenoxathiin and thianthrene have been synthesized and characterized. 1997 Plenum Publishing Corporation.

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