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111354-83-7

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111354-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111354-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,3,5 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 111354-83:
(8*1)+(7*1)+(6*1)+(5*3)+(4*5)+(3*4)+(2*8)+(1*3)=87
87 % 10 = 7
So 111354-83-7 is a valid CAS Registry Number.

111354-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,anthracen-9-ylmethanediol

1.2 Other means of identification

Product number -
Other names 10-diacetoxymethylanthracene

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:111354-83-7 SDS

111354-83-7Relevant articles and documents

Manganese(III)-Mediated Formylation of Aromatic Compounds in the Presence of Malonic Acid

Nishino, Hiroshi,Tsunoda, Katsunori,Kurosawa, Kazu

, p. 545 - 550 (2007/10/02)

The reaction of naphthlenes with malonic acid in the presence of manganese(III) acetate gives naphthalenecarbaldehydes and naphthalenecarboxylic acids.Similar reactions of anthracene, pyrene, and methoxybenzenes also yield formylated and carboxylated products.It was found that the formyl group introduced to the aromatic ring was not derived from carboxymethyl radical generated directly by the thermolysis of manganese(III) acetate, but from a dicarboxymethyl radical formed by the interaction of malonic acid and manganese(III) acetate.In addition, it was also found that the dicarboxymethyl radicals attacked the position of the highest electron density on the aromatic ring and that this formylation was effective when the ionization potential of the aromatic copound was lower than 7.8 eV.

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