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490026-98-7

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490026-98-7 Usage

General Description

MORPHOLIN-4-YL-(4-METHYL)PHENYL-ACETIC ACID is a chemical compound that consists of a morpholine ring attached to a phenyl acetic acid group, with a methyl group located at the 4th position on the phenyl ring. It is often used as a building block in the synthesis of pharmaceutical compounds and agrochemicals. The presence of the morpholine group makes it a potential candidate for the development of drugs with central nervous system (CNS) activity, while the acetic acid moiety enables its use in the production of herbicides and pesticides. Its unique structure and functional groups make MORPHOLIN-4-YL-(4-METHYL)PHENYL-ACETIC ACID a versatile and valuable compound in the field of chemical and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 490026-98-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,0,0,2 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 490026-98:
(8*4)+(7*9)+(6*0)+(5*0)+(4*2)+(3*6)+(2*9)+(1*8)=147
147 % 10 = 7
So 490026-98-7 is a valid CAS Registry Number.

490026-98-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methylphenyl)-2-morpholin-4-ylacetic acid

1.2 Other means of identification

Product number -
Other names M-1768

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:490026-98-7 SDS

490026-98-7Downstream Products

490026-98-7Relevant articles and documents

On the use of boronates in the Petasis reaction

Jourdan, Hélène,Gouhier, Géraldine,Van Hijfte, Luc,Angibaud, Patrick,Piettre, Serge R.

, p. 8027 - 8031 (2007/10/03)

Alcohols are solvents of choice to react boronates, aldehydes and either primary or secondary amines. Thus, while the reaction proceeds sluggishly, or not at all, in aprotic solvents, the desired aminoacids are in most cases obtained in high yields when c

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