3-Methylbutyl amino(phenyl)acetate hydrochloride

Base Information

• Chemical Name: 3-Methylbutyl amino(phenyl)acetate hydrochloride
• CAS No.: 31031-74-0
• Molecular Formula: C₁₃H₁₉NO₂*ClH
• Molecular Weight: 257.76
• Hs Code.: 2922499990
• European Community (EC) Number: 608-572-9
• UNII: 6X7522VT4B
• DSSTox Substance ID: DTXSID80953146
• Wikidata: Q27265658
• Mol file: 31031-74-0.mol

Synonyms:31031-74-0;Aklonin;3-methylbutyl amino(phenyl)acetate hydrochloride;isopentyl amino(phenyl)acetate hydrochloride;Phenamacide (hydrochloride);Phenamacide hydrochloride;3-methylbutyl 2-amino-2-phenylacetate;hydrochloride;Phenamacide HCl;3-METHYLBUTYL 2-AMINO-2-PHENYLACETATE HYDROCHLORIDE;6X7522VT4B;SCHEMBL24243;PHENAMAZIDE HYDROCHLORIDE;DTXSID80953146;MFCD00050708;PHENAMACIDE HYDROCHLORIDE [MI];AKOS024326172;PHENAMAZIDE HYDROCHLORIDE [MART.];PHENAMACIDE HYDROCHLORIDE [WHO-DD];Q27265658;3-Methylbutyl amino(phenyl)acetate--hydrogen chloride (1/1);(+/-)-.ALPHA.-AMINOBENZENEACETIC ACID 3-METHYLBUTYL ESTER HYDROCHLORIDE

Chemical Property of 3-Methylbutyl amino(phenyl)acetate hydrochloride

Chemical Property:

• Vapor Pressure: 0.00096mmHg at 25°C
• Melting Point: 154°
• Boiling Point: 302.9°Cat760mmHg
• Flash Point: 157.9°C
• PSA: 52.32000
• Density: g/cm³
• LogP: 3.77800
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 257.1182566
• Heavy Atom Count: 17
• Complexity: 210

Purity/Quality:

99% ^*data from raw suppliers

AMINO-PHENYL-ACETIC ACID 3-METHYL-BUTYL ESTER, HYDROCHLORIDE Aldrich ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)CCOC(=O)C(C1=CC=CC=C1)N.Cl

Technology Process of 3-Methylbutyl amino(phenyl)acetate hydrochloride

There total 1 articles about 3-Methylbutyl amino(phenyl)acetate hydrochloride 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: 88.0%

i-Amyl alcohol (123-51-3) + phenylglycin (2835-06-5) → Phenamacidum hydrochloricum (31031-74-0)

Guidance literature:

upstream raw materials:

i-Amyl alcohol

phenylglycin

Refernces