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12-Chlorodehydroabietic acide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65310-45-4

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65310-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65310-45-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,1 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65310-45:
(7*6)+(6*5)+(5*3)+(4*1)+(3*0)+(2*4)+(1*5)=104
104 % 10 = 4
So 65310-45-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H27ClO2/c1-12(2)14-10-13-6-7-17-19(3,15(13)11-16(14)21)8-5-9-20(17,4)18(22)23/h10-12,17H,5-9H2,1-4H3,(H,22,23)/t17-,19-,20-/m1/s1

65310-45-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 12-Chloroabieta-8(14),9(11),12-trien-18-oic acid

1.2 Other means of identification

Product number -
Other names 5,12-Naphthacenedione,11-chloro-2,6-dihydroxy

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:65310-45-4 SDS

65310-45-4Upstream product

65310-45-4Downstream Products

65310-45-4Relevant academic research and scientific papers

Studies related to biological detoxification of kraft pulp mill effluent. V. The synthesis of 12- and 14-chlorodehydroabietic acids and 12,14-dichlorodehydroabietic acid, fish-toxic diterpenes from kraft pulp mill effluent

Kutney,Dimitriadis

, p. 1351 - 1358 (1982)

An improved synthesis of the isomeric 12- and 14-chlorodehydroabietic acids and 12,14-dichlorodehydroabietic acid is described. The monochloro isomers were conveniently separated as the imidazole derivatives, and conversion of the latter to the free acids or their corresponding methyl esters could be achieved in high yield.

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