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13560-89-9

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  • 1,4:7,10-Dimethanodibenzo[a,e]cyclooctene,1,2,3,4,7,8,9,10,13,13,14,14-dodecachloro-1,4,4a,5,6,6a,7,10,10a,11,12,12a-dodecahydro- 13560-89-9

    Cas No: 13560-89-9

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13560-89-9 Usage

Chemical Properties

Off-White Solid

Uses

Different sources of media describe the Uses of 13560-89-9 differently. You can refer to the following data:
1. Fire retardant for plastics.
2. A chlorinated polycyclic compound as flame retardant and organochlorine pollutant.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 13560-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,6 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13560-89:
(7*1)+(6*3)+(5*5)+(4*6)+(3*0)+(2*8)+(1*9)=99
99 % 10 = 9
So 13560-89-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H12Cl12/c19-9-10(20)15(25)7-3-4-8-6(2-1-5(7)13(9,23)17(15,27)28)14(24)11(21)12(22)16(8,26)18(14,29)30/h5-8H,1-4H2

13560-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Dechlorane A

1.2 Other means of identification

Product number -
Other names Dechlorane plus

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Flame retardants,Intermediates
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:13560-89-9 SDS

13560-89-9Upstream product

13560-89-9Downstream Products

13560-89-9Relevant articles and documents

Process for the preparation of Diels-Alder adducts of halogenated cyclopentadienes

-

, (2008/06/13)

An improved process for the preparation of solid Diels-Alder adducts of halogenated cyclopentadienes and mono- or diolefins is disclosed wherein the reactants are combined in an aqueous emulsion. The adducts are obtained in excellent yield and in an extremely fine particulate form. The new process avoids the use of organic solvents which are relatively costly, hazardous to use, and from which the adducts are usually obtained as relatively large crystals which require pulverization prior to use.

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