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40476-29-7

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40476-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40476-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,7 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40476-29:
(7*4)+(6*0)+(5*4)+(4*7)+(3*6)+(2*2)+(1*9)=107
107 % 10 = 7
So 40476-29-7 is a valid CAS Registry Number.

40476-29-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-methylidene-9H-anthracene

1.2 Other means of identification

Product number -
Other names Anthracene,9,10-dihydro-9-methylene

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:40476-29-7 SDS

40476-29-7Relevant articles and documents

Photochemical Behaviour of 9-(2-Anilinoethyl)- and 9-(3-Anilinopropyl)anthracenes in Various Solvents

Sugimoto, Akira,Yamano, Junzo,Suyama, Kanji,Yoneda, Shigeo

, p. 483 - 487 (2007/10/02)

Photochemical reactions of the title compounds and related aniline derivatives have been studied in various solvents.Products isolated from an irradiated mixture of 9-(2-anilinoethyl)anthracene (5) were: 9-methylene-9,10-dihydroanthracene (6), N-phenyl-9,

Synthesis of 9-Methylene-9,10-dihydroanthracene by Lithium Aluminium Hydride Reduction of (9-Anthrylmethyl)trimethylammonium Chloride

Takagi, Masato,Hirabe, Tomoatsu,Nojima, Masatomo,Kusabayashi, Shigekazu

, p. 1311 - 1314 (2007/10/02)

Treatment of (9-anthrylmethyl)trimethylammonium chloride (2a) with 1 mol equiv. of lithium aluminium hydride (LAH) in refluxing tetrahydrofuran gave predominantly 9-methylene-9,10-dihydroanthracene (3a).However, reaction with 3 mol equiv. of LAH gave a mixture of 9-methyl-9,10-dihydroantracene (5a) and 9-(9-anthrylmethyl)-9-methyl-9,10-dihydroanthracene (6a), these products being formed by processes involving nucleophilic attack of excess of LAH on compound (3a).

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