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1-Naphthaleneacetic acid, 2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62018-15-9

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62018-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62018-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,1 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62018-15:
(7*6)+(6*2)+(5*0)+(4*1)+(3*8)+(2*1)+(1*5)=89
89 % 10 = 9
So 62018-15-9 is a valid CAS Registry Number.

62018-15-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-phenylnaphthalen-1-yl)acetic acid

1.2 Other means of identification

Product number -
Other names (2-phenyl-[1]naphthyl)-acetic acid

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:62018-15-9 SDS

62018-15-9Upstream product

62018-15-9Downstream Products

62018-15-9Relevant academic research and scientific papers

Ligand-accelerated cross-coupling of C(sp2)-H bonds with arylboron reagents

Engle, Keary M.,Thuy-Boun, Peter S.,Dang, Michael,Yu, Jin-Quan

supporting information; experimental part, p. 18183 - 18193 (2011/12/21)

A ligand-accelerated Pd(II)-catalyzed C(sp2)-H/arylboron cross-coupling reaction of phenylacetic acid substrates is reported. Using Ac-Ile-OH as the ligand and Ag2CO3 as the oxidant, a fast, high-yielding, operationally si

Antiinflammatory activity of isomeric phenylnaphthaleneacetic acids

Kaltenbronn

, p. 596 - 598 (2007/10/13)

The isomeric phenylnaphthaleneacetic acids were prepared and tested for antiinflammatory activity by the anti-UV-erythema method. High potency was exhibited by 4- and 5-phenyl-1 naphthaleneacetic acid and 5- and 6-phenyl-2-naphthaleneacetic acid. The results are discussed in terms of a hypothetical receptor site.

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