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117-05-5

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117-05-5 Usage

Safety Profile

Moderately toxic byintraperitoneal route. An eye irritant. Mutation datareported. When heated to decomposition it emits verytoxic fumes of NOx and Cl-.

Check Digit Verification of cas no

The CAS Registry Mumber 117-05-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 117-05:
(5*1)+(4*1)+(3*7)+(2*0)+(1*5)=35
35 % 10 = 5
So 117-05-5 is a valid CAS Registry Number.
InChI:InChI=1/C21H12ClNO3/c22-15-10-4-8-13-17(15)19(24)14-9-5-11-16(18(14)20(13)25)23-21(26)12-6-2-1-3-7-12/h1-11H,(H,23,26)

117-05-5SDS

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 N-(5-chloro-9,10-dioxoanthracen-1-yl)benzamide

1.2 Other means of identification

Product number -
Other names N-(5-Chloro-9,10-dihydro-9,10-dioxo-1-anthracenyl)benzamide

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:117-05-5 SDS

117-05-5Relevant articles and documents

Process for the preparation of 1-acylamino-5(8)-chloroanthraquinones

-

, (2008/06/13)

The invention relates to a novel process for the preparation of 1-acylamino-5(8)-chloroanthraquinones, which are starting materials for the preparation of vat dyes. It is characterized in that 1,5(8)-dichloroanthraquinones is reacted with ammonia at temperatures of 190° to 240° C., the amino groups in the reaction mixture are completely acylated and the more sparingly soluble diacylaminoanthraquinone is separated off from the more readily soluble monoacylaminochloroanthraquinone. The new process yields reaction products which are purer and cheaper than those which are obtained by conventional methods. Moreover there are smaller waste water problems.

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