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4-chloropyrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73765-17-0

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73765-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73765-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,6 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73765-17:
(7*7)+(6*3)+(5*7)+(4*6)+(3*5)+(2*1)+(1*7)=150
150 % 10 = 0
So 73765-17-0 is a valid CAS Registry Number.

73765-17-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloropyrene

1.2 Other means of identification

Product number -
Other names Pyrene,4-chloro

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:73765-17-0 SDS

73765-17-0Upstream product

73765-17-0Downstream Products

73765-17-0Relevant academic research and scientific papers

Mild chlorination of aromatic compounds with tin(IV) chloride and lead tetraacetate

Muathen, Hussni A.

, p. 8863 - 8866 (2007/10/03)

SnCl4/Pb(OAc)4 acts as a safe source of Cl2 for the chlorination of aromatic compounds. A variety of aromatic compounds are effectively chlorinated with SnCl4/Pb(OAc)4 under mild conditions. The mixture is a selective chlorinating agent, particularly with polyalkylbenzenes, polycyclic aromatic compounds and anisoles.

BINARY PHASE CHLORINATION OF AROMATIC HYDROCARBONS WITH SOLID COPPER(II) CHLORIDE: REACTION MECHANISM.

Tanimoto,Kushioka,Kitagawa,Maruyama

, p. 3586 - 3591 (2007/10/05)

Anthracene is selectively chlorinated with solid copper(II) chloride to give a quantitative yield of 9-chloroanthracene. The tentative reaction mechanisms so far proposed fail to explain the nonreactivity of some other hydrocarbon homologues, e. g. naphthalene and phenanthrene, toward copper(II) chloride. The present study revealed that the oxidative half-wave potentials (E//1/////2//0//x) of all reactive hydrocarbon homologues were less than 1. 26 V. On the basis of this finding the authors postulate a reaction mechanism involving one electron transfer from hydrocarbon to copper(II) chloride.

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