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55-59-4

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55-59-4 Usage

Description

(S)-2-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID, also known as 3,4-Dimethoxy-L-phenylalanine, is an organic compound with a unique structure featuring a phenylalanine backbone and two methoxy groups on the phenyl ring. It is a chiral molecule with the (S)-configuration, which is important for its biological activity and potential applications.

Uses

Used in Pharmaceutical Industry:
(S)-2-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID is used as an intermediate in the synthesis of various pharmaceutical compounds, particularly those with potential neurological or psychiatric applications. Its unique structure and chirality make it a valuable building block for the development of new drugs targeting specific receptors or enzymes in the central nervous system.
Used in Chemical Synthesis:
(S)-2-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID is used as a starting material in the synthesis of peptide-based metal ion sensors. Its incorporation into peptide sequences allows for the development of sensors with high selectivity and sensitivity for detecting specific metal ions, which can be useful in environmental monitoring, medical diagnostics, and other analytical applications.
Used in Research and Development:
(S)-2-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID is also used as a research tool in the study of enzyme mechanisms, receptor binding, and other biological processes. Its unique structure and chirality make it an interesting probe for investigating the stereoselectivity of enzymes and the role of chirality in molecular recognition.

Check Digit Verification of cas no

The CAS Registry Mumber 55-59-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55-59:
(4*5)+(3*5)+(2*5)+(1*9)=54
54 % 10 = 4
So 55-59-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO4/c1-15-9-4-3-7(6-10(9)16-2)5-8(12)11(13)14/h3-4,6,8H,5,12H2,1-2H3,(H,13,14)/t8-/m0/s1

55-59-4SDS

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-amino-3-(3,4-dimethoxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names 2-azanyl-3-(3,4-dimethoxyphenyl)propanoic 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:55-59-4 SDS

55-59-4Relevant articles and documents

Bio-inspired enantioselective full transamination using readily available cyclodextrin

Zhang, Shiqi,Li, Guangxun,Liu, Hongxin,Wang, Yingwei,Cao, Yuan,Zhao, Gang,Tang, Zhuo

, p. 4203 - 4208 (2017/02/05)

The mimics of vitamin B6-dependent enzymes that catalyzed an enantioselective full transamination in the pure aqueous phase have been realized for the first time through the establishment of a new “pyridoxal 5′-phosphate (PLP) catalyzed non-covalent cyclodextrin (CD)-keto acid inclusion complexes” system, and various optically active amino acids have been obtained.

Studies on theoretical psychotogens. Synthesis of O methylated analogs of catecholamine neurotransmitters and metabolic precursors

Butterick,Unrau

, p. 2873 - 2879 (2007/10/05)

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