271583-17-6

Basic information

• Product Name: AMINO-(2-METHOXY-PHENYL)-ACETIC ACID
• Synonyms: ALPHA-AMINO-(2-METHOXYPHENYL)ACETIC ACID;VITAS-BB TBB000094;2-aMino-2-(2-Methoxyphenyl)acetic acid;2-(2-Methoxyphenyl)glycine;alpha-Amino-2-methoxybenzeneacetic acid;(2R)-2-azaniuMyl-2-(2-Methoxyphenyl)acetate;2-Amino-2-(2-methoxyphenyl);RS-2-methoxyphenylglycine
• CAS NO: 271583-17-6
• Molecular Formula: C₉H₁₁NO₃
• Molecular Weight: 181.19
• Product Categories: pharmacetical
• Mol File: 271583-17-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 343.9°Cat760mmHg
• Flash Point: 161.8°C
• Appearance: /
• Density: 1.246g/cm³
• Vapor Pressure: 2.6E-05mmHg at 25°C
• Refractive Index: 1.568
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 1.78±0.10(Predicted)
• CAS DataBase Reference: AMINO-(2-METHOXY-PHENYL)-ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: AMINO-(2-METHOXY-PHENYL)-ACETIC ACID(271583-17-6)
• EPA Substance Registry System: AMINO-(2-METHOXY-PHENYL)-ACETIC ACID(271583-17-6)

Safety Data

• Hazardous Substances Data: 271583-17-6(Hazardous Substances Data)

Usage

General Description

Amino-(2-methoxy-phenyl)-acetic acid, also known as o-anisidine, is an organic compound typically used in various chemical applications such as dye production. It consists of an amino group (NH2), a methoxy group (OCH3), and an acetic acid component (CH3COOH) attached to a phenyl ring. The compound is regarded as hazardous, as it has been linked to mutagenic and carcinogenic effects. Therefore, proper safety measures should be strictly observed when handling, storing, and disposing of it. It is soluble in alcohol, ether, and water, appearing as a colorless to slightly yellow liquid or solid in its pure unstable state. It should be stored in an area with good ventilation, away from heat sources or sparks.

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-/m1/s1

Upstream product

• 77651-54-8 5-(2-methoxyphenyl)imidazolidine-2,4-dione 
• 271583-23-4 2-(benzylamino)-2-(2-methoxyphenyl)acetic acid 
• 135-02-4 ortho-anisaldehyde 
• 271583-59-6 2-(benzylamino)-2-(2-methoxyphenyl)acetonitrile 
• 271583-39-2 2-(benzylamino)-2-(2-methoxyphenyl)acetamide 
• 77651-55-9 2-methoxy phenylglycine methyl ester 

Downstream Products

• 77651-55-9 2-methoxy phenylglycine methyl ester 
• 475475-36-6 [formyl-(2-oxo-ethyl)-amino]-(2-methoxy-phenyl)-acetic acid methyl ester 
• 475475-35-5 (2,2-dimethoxy-ethylamino)-(2-methoxy-phenyl)-acetic acid methyl ester 
• 791630-83-6 [(2,2-dimethoxy-ethyl)-formyl-amino]-(2-methoxy-phenyl)-acetic acid methyl ester 
• 475475-37-7 [formyl-(2-{[methoxycarbonyl-(4-methoxy-phenyl)-methyl]-amino}-ethyl)-amino]-(2-methoxy-phenyl)-acetic acid methyl ester 
• 77651-57-1 (2-Methoxy-phenyl)-methylsulfanylmethyleneamino-acetic acid methyl ester 
• 77651-56-0 methyl (+/-)-2-methoxy-α-<(thioxomethyl)amino>benzene acetate 
• 179417-69-7 tert-butoxy-carbonylamino-(2-methoxy-phenyl)-acetic acid 
• 30114-20-6 2-(2-methoxy-phenyl)-4-methyl-quinazoline 

Relevant articles and documents

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

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 facile synthesis of substituted phenylglycines

A convenient scaleable process for the preparation of substituted phenylglycines 2 by a modified Strecker reaction is described. Bisulfite- mediated addition of benzylamine and cyanide anion to substituted benzaldehydes 3 gave the aminonitriles 4 which were hydrolysed in two steps to the N-protected amino acid 1. Debenzylation using catalytic transfer hydrogenation gave the title compounds in good yield.