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1-Naphthaleneacetic acid, 5-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

4022-51-9

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4022-51-9 Usage

Type

Plant growth regulator

Function

Promotes growth and development of plants

Mimics

Natural plant hormone auxin

Usage in agriculture

Stimulates rooting of cuttings, promotes fruit setting, improves quality and yield of fruits and vegetables

Usage in horticulture

Encourages growth of flowers and ornamental plants

Additional use

Can be used as a herbicide to control certain weeds.

Check Digit Verification of cas no

The CAS Registry Mumber 4022-51-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,2 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4022-51:
(6*4)+(5*0)+(4*2)+(3*2)+(2*5)+(1*1)=49
49 % 10 = 9
So 4022-51-9 is a valid CAS Registry Number.

4022-51-9SDS

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-(5-phenylnaphthalen-1-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 1-Naphthaleneacetic acid,5-phenyl

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:4022-51-9 SDS

4022-51-9Upstream product

4022-51-9Downstream Products

4022-51-9Relevant academic research and scientific papers

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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