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103889-86-7

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103889-86-7 Usage

Description

(S)-AMINO-(2-METHOXY-PHENYL)-ACETIC ACID, also known as a homochiral α-arylglycine, is an organic compound that can be asymmetrically synthesized from substituted aryl trichloromethyl ketones and CBS-catecholborane reagent. It is characterized by its white powder form and is known for its unique chemical properties.

Uses

Used in Pharmaceutical Industry:
(S)-AMINO-(2-METHOXY-PHENYL)-ACETIC ACID is used as an intermediate in the synthesis of various pharmaceutical compounds for its ability to be asymmetrically synthesized, allowing for the creation of specific enantiomers with desired biological activities.
Used in Chemical Synthesis:
In the field of chemical synthesis, (S)-AMINO-(2-METHOXY-PHENYL)-ACETIC ACID serves as a key building block for the development of novel molecules with potential applications in various industries, including materials science, agrochemicals, and specialty chemicals.
Used in Research and Development:
(S)-AMINO-(2-METHOXY-PHENYL)-ACETIC ACID is utilized as a research compound for studying its properties and potential applications in different fields. Its unique structure and synthetic accessibility make it an attractive candidate for exploring new reactions and developing innovative chemical processes.
Used in Chiral Pool Synthesis:
As a homochiral α-arylglycine, (S)-AMINO-(2-METHOXY-PHENYL)-ACETIC ACID is used in chiral pool synthesis, a strategy that involves the use of chiral compounds as starting materials to create enantiomerically pure products. This application is particularly relevant in the development of enantiomerically pure drugs, which can have significant implications for their safety and efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 103889-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,8,8 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103889-86:
(8*1)+(7*0)+(6*3)+(5*8)+(4*8)+(3*9)+(2*8)+(1*6)=147
147 % 10 = 7
So 103889-86-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO3/c1-13-7-5-3-2-4-6(7)8(10)9(11)12/h2-5,8H,10H2,1H3,(H,11,12)/t8-/m0/s1

103889-86-7SDS

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 (2S)-2-amino-2-(2-methoxyphenyl)acetic acid

1.2 Other means of identification

Product number -
Other names -

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:103889-86-7 SDS

103889-86-7Relevant articles and documents

ISOINDOLIN-1-ON DERIVATIVE, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION COMPRISING SAME AS EFFECTIVE COMPONENT FOR PREVENTING OR TREATING CANCER

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Paragraph 0092; 0094, (2021/06/25)

The present invention relates to an isoindolin-1-one derivative, a method for preparing the same, and a pharmaceutical composition comprising the same as an active ingredient for preventing or treating cancer, wherein the isoindolin-1-one derivative exhib

A practical asymmetric synthesis of homochiral α-arylglycines

Mellin-Morliere, Christelle,Aitken, David J.,Bull, Steven D.,Davies, Stephen G.,Husson, Henri-Philippe

, p. 149 - 155 (2007/10/03)

Enantioselective reduction of a series of substituted aryl trichloromethyl ketones with the CBS-catecholborane reagent afforded homochiral aryl trichloromethyl carbinols which have been elaborated to give homochiral α-arylglycines in high e.e.

SYNTHESIS OF 2,3-BENZO-1-OXAOCTEM-4-CARBOXYLIC ACID

Daum, S. J.,Hansen, P. E.

, p. 1 - 6 (2007/10/02)

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