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25308-63-8

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25308-63-8 Usage

General Description

2-Phenanthrenecarboxylic acid methyl ester is a chemical compound that belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic aromatic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene rings. The methyl ester variant of this chemical means it includes a methoxy group (a carbon atom bonded to three hydrogen atoms and one oxygen atom). Its applications and uses are mainly in scientific research. This chemical can be synthesized in a lab, and it's useful for the synthesis of other complex chemical compounds. Its exact toxicity and safety measures are not well studied and may vary based on the quantity and exposure type.

Check Digit Verification of cas no

The CAS Registry Mumber 25308-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,0 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25308-63:
(7*2)+(6*5)+(5*3)+(4*0)+(3*8)+(2*6)+(1*3)=98
98 % 10 = 8
So 25308-63-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O2/c1-18-16(17)13-8-9-15-12(10-13)7-6-11-4-2-3-5-14(11)15/h2-10H,1H3

25308-63-8SDS

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 methyl phenanthrene-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Phenanthrenecarboxylicacid,methyl ester

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:25308-63-8 SDS

25308-63-8Relevant articles and documents

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Dixon,J.A.,Neiswender,D.D.

, p. 499 - 503 (1960)

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1-Phenylisobenzofuran, 1-Phenylnaphthofuran, 1-Phenylnaphthofuran, and 3-Phenylnaphthofuran via Cyclic Hemiaminal, Hemiacetal, and Acetal Precursors

Smith, James G.,Fogg, Deryn E.,Munday, Ian J.,Sandborn, Richard E.,Dibble, Peter W.

, p. 2942 - 2953 (2007/10/02)

The title compounds have been generated via cyclic hemiaminal, hemiacetal, and acetal precursors and trapped in Diels-Alder reactions with several dienophiles.The precursors are easily prepared from o-bromobenzyl alcohol, 2-bromo-3-naphthalenemethanol, or

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