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70494-48-3

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70494-48-3 Usage

General Description

(S)-3,4-DIMETHOXYPHENYLALANINE METHYL ESTER HYDROCHLORIDE is a chemical compound that contains an amino acid derivative and a methyl ester group. It is commonly used in organic synthesis and pharmaceutical research. (S)-3,4-DIMETHOXYPHENYLALANINE METHYL ESTER HYDROCHLORIDE has potential applications in the development of new drugs and as a building block in the synthesis of complex organic molecules. Additionally, it may have biological activity and could be used in the study of various biochemical processes. Its hydrochloride form suggests that it is a salt of the compound, making it more stable and soluble in water.

Check Digit Verification of cas no

The CAS Registry Mumber 70494-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,9 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70494-48:
(7*7)+(6*0)+(5*4)+(4*9)+(3*4)+(2*4)+(1*8)=133
133 % 10 = 3
So 70494-48-3 is a valid CAS Registry Number.

70494-48-3SDS

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 methyl (2S)-2-amino-3-(3,4-dimethoxyphenyl)propanoate

1.2 Other means of identification

Product number -
Other names (S)-(+)-3,4-dimethoxyphenylalanine methyl ester hydrochloride

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:70494-48-3 SDS

70494-48-3Relevant articles and documents

Substituted Dihydroisoquinolinones by Iodide-Promoted Cyclocarbonylation of Aromatic α-Amino Acids

Amer, Mostafa M.,Carrasco, Ana C.,Leonard, Daniel J.,Ward, John W.,Clayden, Jonathan

supporting information, p. 7977 - 7981 (2019/01/04)

Imidazolidinone derivatives of a range of aromatic α-amino acids, on treatment with phosgene and potassium iodide, undergo a mild Bischler-Napieralski-style cyclocarbonylation reaction that generates a tricyclic lactam by insertion of a C=O group between amino acid nitrogen and the ortho position of the aryl substituent. Regio- and diastereoselective functionalization of the lactam generates a library of substituted dihydroisoquinolinones and their congeners in enantioenriched form.

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