Sodium methoxyacetate

Base Information

• Chemical Name: Sodium methoxyacetate
• CAS No.: 50402-70-5
• Deprecated CAS: 1158305-07-7
• Molecular Formula: C3H5NaO3
• Molecular Weight: 112.061
• Hs Code.: 2918990090
• European Community (EC) Number: 256-578-1
• DSSTox Substance ID: DTXSID60885911
• Nikkaji Number: J134.861B
• Wikidata: Q27225411
• Mol file: 50402-70-5.mol

Synonyms:Sodium methoxyacetate;50402-70-5;Acetic acid, methoxy-, sodium salt;Methoxyacetic acid sodium salt;sodium;2-methoxyacetate;EINECS 256-578-1;Acetic acid, 2-methoxy-, sodium salt (1:1);SCHEMBL630881;Methoxy-acetic acid, sodium salt;DTXSID60885911;CEWQOBFWNPUNRO-UHFFFAOYSA-M;CHEBI:132096;AKOS003052999;AKOS022190862;LS-185136;Q27225411

Chemical Property of Sodium methoxyacetate

Chemical Property:

• Vapor Pressure: 0.131mmHg at 25°C
• Boiling Point: 201°C at 760 mmHg
• Flash Point: 94°C
• PSA: 49.36000
• LogP: -1.61730
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 112.01363830
• Heavy Atom Count: 7
• Complexity: 54.1

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COCC(=O)[O-].[Na+]

Technology Process of Sodium methoxyacetate

There total 1 articles about Sodium methoxyacetate 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:

(R)-2-methoxy-N-(1-phenylethyl)acetamide (162929-44-4) → (R)-1-phenyl-ethyl-amine (3886-69-9) + methoxyacetic acid sodium salt (50402-70-5)

Guidance literature:

With sodium hydroxide;

Reference yield: 27.0%

chloro(phenylimino)methyl trichloromethyl sulphide (79963-68-1) + methoxyacetic acid sodium salt (50402-70-5) → (2-Methoxy-acetyl)-phenyl-thiocarbamic acid S-trichloromethyl ester

Guidance literature:

With Aliquat 336; In water; benzene; for 3h; Heating; further phase-transfer catalysts (benzyltriethylammonoium chloride, hexadecyltrimethylammonium bromide); further solvent - light petroleum ether;

Reference yield:

methoxyacetic acid sodium salt (50402-70-5) → 2-methoxyacetic acid (625-45-6)

Guidance literature:

With sulfuric acid; In water; at 20 - 65 ℃; pH=1;

upstream raw materials:

(R)-2-methoxy-N-(1-phenylethyl)acetamide

Downstream raw materials:

O-Methoxyacetyl-N-aethyl-salicylamid

rac-1-(4-methoxyphenyl)-ethanol

1-methoxy-4-(1-methoxy-ethyl)-benzene

1-(4-methoxyphenyl)ethyl trifluoroethyl ether

Refernces