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Morpholin-3-yl-acetic acid (MAA) is a white crystalline solid chemical compound characterized by a morpholine ring and a carboxylic acid group. It is widely recognized for its role as a reagent in organic synthesis and pharmaceutical research, with potential applications in the development of drugs for treating a range of conditions including cancer, infectious diseases, and neurological disorders. MAA also serves as an intermediate in the production of various chemicals, such as surfactants, polymers, and agricultural products, and is valued for its antimicrobial properties, which find utility in personal care and household products.

86236-84-2

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86236-84-2 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
Morpholin-3-yl-acetic acid is used as a reagent in pharmaceutical research for the development of drugs targeting cancer, infectious diseases, and neurological disorders. Its unique chemical structure allows for the creation of new drug candidates that can potentially treat these conditions more effectively.
Used in Chemical Production:
MAA is used as an intermediate in the production of various chemicals, including surfactants, polymers, and agricultural products. Its versatility in chemical reactions makes it a valuable component in the synthesis of a wide range of compounds.
Used in Personal Care and Household Products:
Morpholin-3-yl-acetic acid is used as an antimicrobial ingredient in certain personal care and household products. Its ability to inhibit the growth of microorganisms contributes to the preservation and safety of these products, enhancing their shelf life and effectiveness.
Used in Antimicrobial Applications:
In the field of antimicrobial applications, MAA is utilized for its antimicrobial properties, which are beneficial in controlling microbial growth in various settings, from healthcare to consumer products, ensuring cleanliness and reducing the risk of infection.

Check Digit Verification of cas no

The CAS Registry Mumber 86236-84-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,3 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86236-84:
(7*8)+(6*6)+(5*2)+(4*3)+(3*6)+(2*8)+(1*4)=152
152 % 10 = 2
So 86236-84-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO3/c8-6(9)3-5-4-10-2-1-7-5/h5,7H,1-4H2,(H,8,9)

86236-84-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-morpholin-3-ylacetic acid

1.2 Other means of identification

Product number -
Other names Morpholine-3-yl-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:86236-84-2 SDS

86236-84-2Relevant academic research and scientific papers

Enzymatic resolution of cyclic N-Boc protected β-aminoacids

Pousset, Cyrille,Callens, Roland,Haddad, Mansour,Larcheveque, Marc

, p. 3407 - 3412 (2007/10/03)

Methyl and ethyl esters of N-Boc homoproline, homopipecolic acid and 3-carboxymethyl-morpholine were kinetically resolved by hydrolysis catalysed by Burkholderia cepacia lipase to give the corresponding acids and residual esters in enantiomeric excesses better than 99% (E > 100).

Decarboxylation Reaction. X. Introduction of a Carbon unit at the α-Position of Amines by Reaction of Hexahydro-1,3,5-triazines with Carboxylic Acids

Fukawa, Hidemichi,Terao, Yoshiyasu,Achiwa, Kazuo,Sehiya, Minoru

, p. 94 - 99 (2007/10/02)

An efficient method for introducing a carbon unit at the α-position of alicyclic amines is described.The method involves the reaction of monocyclic or tetracyclic hexahydro-1,3,5-triazines with trichloroacetic acid, cyanoacetic acid, malonic acid and their derivatives, which are introduced into the α-position of amines in the decarboxylated form.Keywords --- 1,3,5-trialkylhexahydro-1,3,5-triazine; trimer of alicyclic imine; decarboxylation; β-amino acid; carboxylic acid

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