2-(2-propylpentanoylamino)acetic Acid

Base Information

Chemical Name:2-(2-propylpentanoylamino)acetic Acid
CAS No.:88321-07-7
Molecular Formula:C₁₀H₁₉NO₃
Molecular Weight:201.266
Hs Code.:
DSSTox Substance ID:DTXSID40236962
Nikkaji Number:J457.079K
Wikidata:Q83119046
Metabolomics Workbench ID:42209

Synonyms:2-(2-propylpentanoylamino)acetic Acid;Valproylglycine;88321-07-7;N-Valproylglycine;(2-Propylpentanoyl)glycine;valproyl glycine;starbld0045340;SCHEMBL4017322;DTXSID40236962;N-(2-propyl-n-pentanoyl)glycine;CHEBI:171680;2-(2-propylpentanamido)acetic acid;N-(2-n-propyl-n-pentanoyl)glycine;KN-539;AKOS026124155;HY-W141935;CS-0201726;N-Valproylglycine, analytical reference material;Z1508928286

Suppliers and Price of 2-(2-propylpentanoylamino)acetic 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

Total 0 raw suppliers

Chemical Property of 2-(2-propylpentanoylamino)acetic Acid

Chemical Property:

Vapor Pressure:2.17E-07mmHg at 25°C
Boiling Point:396.4°Cat760mmHg
Flash Point:193.5°C
Density:1.034g/cm³
XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:201.13649347
Heavy Atom Count:14
Complexity:186

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC(CCC)C(=O)NCC(=O)O

Technology Process of 2-(2-propylpentanoylamino)acetic Acid

There total 5 articles about 2-(2-propylpentanoylamino)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: 59.0%

: 2936-08-5
valproyl chloride

: 56-40-6,18875-39-3,25718-94-9
glycine

: 88321-07-7
Valproylglycine

Guidance literature:: With hydrogenchloride; sodium hydroxide; In water; ethyl acetate;

Reference yield:

: N^α-valproyl glycine ethyl ester

: 88321-07-7
Valproylglycine

Guidance literature:: N^α-valproyl glycine ethyl ester; With water; sodium hydroxide; In methanol; at -5 ℃;

With hydrogenchloride; In methanol; water; at 4 ℃; pH=Ca. 3;

Reference yield:

: 99-66-1
valproic acid

: 88321-07-7
Valproylglycine

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / dichloromethane / 0.33 h / -20 °C

2.1: dichloromethane / 15 h / -20 - 20 °C / pH Ca_.7.5

3.1: sodium hydroxide; water / methanol / -5 °C

3.2: 4 °C / pH Ca_. 3

With water; triethylamine; sodium hydroxide; In methanol; dichloromethane;