(3,5-Dimethoxy-benzoylamino)-acetic acid

Base Information

• Chemical Name: (3,5-Dimethoxy-benzoylamino)-acetic acid
• CAS No.: 62098-74-2
• Molecular Formula: C11H13NO5
• Molecular Weight: 239.22500
• DSSTox Substance ID: DTXSID00368354
• Wikidata: Q82154824

Synonyms:62098-74-2;(3,5-Dimethoxy-benzoylamino)-acetic acid;2-[(3,5-dimethoxybenzoyl)amino]acetic Acid;N-(3,5-dimethoxybenzoyl)glycine;2-[(3,5-dimethoxyphenyl)formamido]acetic acid;2-(3,5-Dimethoxybenzamido)acetic acid;Glycine, N-(3,5-dimethoxybenzoyl)-;DTXSID00368354;CHEBI:168859;MFCD03964570;STK696189;2-(3,5-Dimethoxybenzamido)aceticacid;AKOS000116567;(3,5-dimethoxybenzoylamino)acetic acid;NCGC00331551-01;LS-07944;N-[(3,5-dimethoxyphenyl)carbonyl]glycine;CS-0219682;EN300-04673;AB01324605-02;SR-01000039467;J-501106;SR-01000039467-1;Z56886326;N-(3,5-DimethoxybenZoyl)glycine (BZ(3,5-diOMe)-Gly-OH);2-{[(3,5-dimethoxyphenyl)(hydroxy)methylidene]amino}acetic acid

Chemical Property of (3,5-Dimethoxy-benzoylamino)-acetic acid

Chemical Property:

• PSA: 88.35000
• LogP: 1.09300
• XLogP3: 0.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 5
• Exact Mass: 239.07937252
• Heavy Atom Count: 17
• Complexity: 269

Purity/Quality:

99% ^*data from raw suppliers

(3,5-DIMETHOXY-BENZOYLAMINO)-ACETIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC(=CC(=C1)C(=O)NCC(=O)O)OC

Technology Process of (3,5-Dimethoxy-benzoylamino)-acetic acid

There total 2 articles about (3,5-Dimethoxy-benzoylamino)-acetic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 72.0%

3,5-dimethoxybenzoyl chloride (17213-57-9) + glycine (56-40-6,18875-39-3,25718-94-9) → {[(3,5-dimethoxyphenyl)carbonyl]amino}acetic acid (62098-74-2)

Guidance literature:

With sodium hydroxide; In water; at 25 ℃;

DOI:10.1002/jhet.2786

Reference yield:

3,5-dimethoxybenzoic acid (1132-21-4) → {[(3,5-dimethoxyphenyl)carbonyl]amino}acetic acid (62098-74-2)

Guidance literature:

Multi-step reaction with 2 steps

1: thionyl chloride / 4 h / 80 °C

2: sodium hydroxide / 0.5 h / 0 °C

With thionyl chloride; sodium hydroxide;

DOI:10.1111/cbdd.12774

Reference yield:

{[(3,5-dimethoxyphenyl)carbonyl]amino}acetic acid (62098-74-2) → C23H25FN2O4

Guidance literature:

Multi-step reaction with 2 steps

1: potassium acetate; acetic anhydride / 1 h / Reflux

2: dichloromethane / 1 h / 0 °C

With potassium acetate; acetic anhydride; In dichloromethane;

DOI:10.1111/cbdd.12774

upstream raw materials:

3,5-dimethoxybenzoyl chloride

glycine

3,5-dimethoxybenzoic acid

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