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2-[(4-methylnaphthalen-1-yl)methyl]benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

7248-49-9

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7248-49-9 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 72, p. 264, 1950 DOI: 10.1021/ja01157a072

Check Digit Verification of cas no

The CAS Registry Mumber 7248-49-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,4 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7248-49:
(6*7)+(5*2)+(4*4)+(3*8)+(2*4)+(1*9)=109
109 % 10 = 9
So 7248-49-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H16O2/c1-13-10-11-15(17-8-5-4-7-16(13)17)12-14-6-2-3-9-18(14)19(20)21/h2-11H,12H2,1H3,(H,20,21)

7248-49-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-methylnaphthalen-1-yl)methyl]benzoic acid

1.2 Other means of identification

Product number -
Other names -

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:7248-49-9 SDS

7248-49-9Downstream Products

7248-49-9Relevant academic research and scientific papers

Synthesis of Annulated Anthracenes, Carbazoles, and Thiophenes Involving Bradsher-Type Cyclodehydration or Cyclization-Reductive-Dehydration Reactions

Rafiq, Settu Muhamad,Sivasakthikumaran, Ramakrishnan,Karunakaran, Jayachandran,Mohanakrishnan, Arasambattu K.

, p. 5099 - 5114 (2015/08/18)

A conventional BF3·OEt2-mediated Bradsher-type cyclodehydration of 2-arylmethyl benzaldehydes in CH2Cl2 at room temperature gave polycyclic aromatic and heteroaromatic compounds. Alternatively, these compounds could be synthesized in better yields from 2-arylmethylbenzoic acids by triflic-acid-mediated cyclization followed by reductive dehydration.

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