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55383-92-1

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55383-92-1 Usage

General Description

Methyl 3-(4-Methoxybenzylamino)propanoate is a chemical compound with the molecular formula C12H17NO3. It is an ester derivative of propanoic acid with a methyl group and a 4-methoxybenzylamino group attached to the carbon chain. Methyl 3-(4-MethoxybenzylaMino)propanoate is often used in the pharmaceutical industry as an intermediate in the synthesis of various organic compounds, including potential drug candidates or active pharmaceutical ingredients. The 4-methoxybenzylamino group is often used as a protective group in organic synthesis to prevent unwanted reactions. The compound may also be used in research or laboratory settings as a reagent in chemical reactions or as a reference standard for analytical purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 55383-92-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,8 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55383-92:
(7*5)+(6*5)+(5*3)+(4*8)+(3*3)+(2*9)+(1*2)=141
141 % 10 = 1
So 55383-92-1 is a valid CAS Registry Number.

55383-92-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-[(4-methoxyphenyl)methylamino]propanoate

1.2 Other means of identification

Product number -
Other names SC3391

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:55383-92-1 SDS

55383-92-1Relevant articles and documents

Aza-Michael mono-addition using acidic alumina under solventless conditions

Bosica, Giovanna,Abdilla, Roderick

, (2016/07/07)

Aza-Michael reactions between primary aliphatic and aromatic amines and various Michael acceptors have been performed under environmentally-friendly solventless conditions using acidic alumina as a heterogeneous catalyst to selectively obtain the corresponding mono-adducts in high yields. Ethyl acrylate was the main acceptor used, although others such as acrylonitrile, methyl acrylate and acrylamide were also utilized successfully. Bi-functional amines also gave the mono-adducts in good to excellent yields. Such compounds can serve as intermediates for the synthesis of anti-cancer and antibiotic drugs.

Lipase-catalyzed aza-michael reaction on acrylate derivatives

Steunenberg, Peter,Sijm, Maarten,Zuilhof, Han,Sanders, Johan P. M.,Scott, Elinor L.,Franssen, Maurice C. R.

, p. 3802 - 3813 (2013/06/05)

A methodology has been developed for an efficient and selective lipase-catalyzed aza-Michael reaction of various amines (primary and secondary) with a series of acrylates and alkylacrylates. Reaction parameters were tuned, and under the optimal conditions it was found that Pseudomonas stutzeri lipase and Chromobacterium viscosum lipase showed the highest selectivity for the aza-Michael addition to substituted alkyl acrylates. For the first time also, some CLEAs were examined that showed a comparable or higher selectivity and yield than the free enzymes and other formulations.

COMPOUNDS AND METHODS FOR THE TREATMENT OR PREVENTION OF FLAVIVIRUS INFECTIONS

-

Page 130, (2010/02/07)

The present invention provides novel compounds represented by formula (I) or pharmaceutically acceptable salts thereof useful for treating flaviviridae viral infection.

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