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4022-43-9

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4022-43-9 Usage

Type of compound

Organic

Derivative

Naphthaleneacetic acid

Plant hormone

Regulates growth and development of plants

Effects on plant growth

Potentially promotes root formation, increases flower and fruit production

Agricultural use

Growth regulator for various crops

Safety precautions

Handle carefully and follow guidelines to avoid negative effects on human health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 4022-43-9 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, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4022-43:
(6*4)+(5*0)+(4*2)+(3*2)+(2*4)+(1*3)=49
49 % 10 = 9
So 4022-43-9 is a valid CAS Registry Number.

4022-43-9SDS

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

1.2 Other means of identification

Product number -
Other names 1-Naphthaleneacetic acid,4-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:4022-43-9 SDS

4022-43-9Relevant articles and documents

Rational design of a pirinixic acid derivative that acts as subtype-selective PPARγ modulator

Thieme, Theresa M.,Steri, Ramona,Proschak, Ewgenij,Paulke, Alexander,Schneider, Gisbert,Schubert-Zsilavecz, Manfred

supporting information; scheme or table, p. 2469 - 2473 (2010/07/16)

Peroxisome proliferator-activated receptor γ (PPARγ) is involved in glucose and lipid homeostasis. PPARγ agonists are in clinical use for the treatment of type 2 diabetes. Lately, a new class of selective PPARγ modulators (SPPARγMs) was developed, which are believed to show less side effects than full PPARγ agonists. We have previously shown that α-substitution of pirinixic acid, a moderate agonist of PPARα and PPARγ, leads to low micromolar active balanced dual agonists of PPARα and PPARγ. Herein we present modifications of pirinixic acid leading to subtype-selective PPARγ agonists and furthermore the development of a selective PPARγ modulator guided by molecular docking studies.

4- and 5-Aryl-l-naphthaleneacetic acids as antiinflammatory agents.

Kaltenbronn

, p. 490 - 493 (2007/10/13)

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