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9-Methyl-10-(chloromethyl)anthracene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25148-26-9

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25148-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25148-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,4 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25148-26:
(7*2)+(6*5)+(5*1)+(4*4)+(3*8)+(2*2)+(1*6)=99
99 % 10 = 9
So 25148-26-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H13Cl/c1-11-12-6-2-4-8-14(12)16(10-17)15-9-5-3-7-13(11)15/h2-9H,10H2,1H3

25148-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(chloromethyl)-10-methylanthracene

1.2 Other means of identification

Product number -
Other names ANTHRACENE,10-CHLOROMETHYL-9-METHYL

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:25148-26-9 SDS

25148-26-9Relevant academic research and scientific papers

MUTUAL TRANSFORMATIONS OF THE DICATIONS OF ALKYL AROMATIC COMPOUNDS AND THEIR CONJUGATE CATIONS OF BENZYL TYPE

Bodoev, N.V.,Krysin, A.P.,Koptyug, V.A.

, p. 880 - 885 (2007/10/02)

For ions of the anthracene and naphthalene series it was only possible to observe transitions betveen the dications of alkyl aromatic compounds (2+) and cations of the benzyl type ArCH(+)R (R = CH3, H), which are conjugated acids and bases, for the case of the thermodynamically favorable transformation of the dication into the conjugate monocation.Even if it is favorable in thermodynamic respects, the reverse transformation involves overcoming a high activation barrier, which is evidently due to electrostatic repulsion of the proton and of the positively charged center being protonated.

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