N-Salicyloylaspartic acid

Base Information

Chemical Name:N-Salicyloylaspartic acid
CAS No.:56145-94-9
Molecular Formula:C₁₁H₁₁NO₆
Molecular Weight:253.211
Hs Code.:2924299090
European Community (EC) Number:660-349-5
Metabolomics Workbench ID:48556
Wikidata:Q105131479

Synonyms:N-Salicyloylaspartic acid;N-(2-Hydroxybenzoyl)-L-aspartic acid;2-[(2-hydroxybenzoyl)amino]butanedioic acid;N-Salicyloyl-Aspartic acid;SCHEMBL18277717;CHEBI:169113;MFCD00157781;AKOS020220472;SY272657;2-[(2-hydroxyphenyl)formamido]butanedioic acid;Z1465345621

Suppliers and Price of N-Salicyloylaspartic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
N-(2-HYDROXYBENZOYL)-L-ASPARTIC ACID 95.00%
5MG
$ 808.57

Total 2 raw suppliers

Chemical Property of N-Salicyloylaspartic acid

Chemical Property:

Vapor Pressure:7.62E-12mmHg at 25°C
Boiling Point:524.9°C at 760 mmHg
Flash Point:271.2°C
PSA：127.42000
Density:1.512g/cm³
LogP:0.62470
XLogP3:0.5
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:253.05863707
Heavy Atom Count:18
Complexity:342

Purity/Quality:

99% ^*data from raw suppliers

N-(2-HYDROXYBENZOYL)-L-ASPARTIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C(=O)NC(CC(=O)O)C(=O)O)O

Technology Process of N-Salicyloylaspartic acid

There total 4 articles about N-Salicyloylaspartic 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: 21.0%

: 617-45-8,25608-40-6,27881-03-4,32505-46-7,52526-39-3
aspartic Acid

: 5538-51-2
O-acetylsalicyloyl chloride

: 56145-94-9
salicyloylaspartate

Guidance literature:: With sodium hydroxide; at 50 ℃; for 0.5h;
DOI:10.1016/0031-9422(91)83462-T

Reference yield:

: 50-78-2,98201-60-6
aspirin

: 56145-94-9
salicyloylaspartate

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂

2: 21 percent / 2 M NaOH / 0.5 h / 50 °C

With sodium hydroxide; thionyl chloride;
DOI:10.1016/0031-9422(91)83462-T