N-[1-(aminocarbonyl)-3-methylbutyl]benzamide

Base Information

• Chemical Name: N-[1-(aminocarbonyl)-3-methylbutyl]benzamide
• CAS No.: 24250-71-3
• Molecular Formula: C₁₃H₁₈N₂O₂
• Molecular Weight: 234.298
• NSC Number: 164653,164030
• Mol file: 24250-71-3.mol

Synonyms:NSC164653;Oprea1_573800;16709-42-5;SCHEMBL17822178;NSC164030;AKOS002980179;NSC-164030;NSC-164653;24250-71-3;N-[1-(aminocarbonyl)-3-methylbutyl]benzamide

Chemical Property of N-[1-(aminocarbonyl)-3-methylbutyl]benzamide

Chemical Property:

• Vapor Pressure: 2.43E-09mmHg at 25°C
• Boiling Point: 479.1°C at 760 mmHg
• Flash Point: 243.6°C
• Density: 1.095g/cm³
• XLogP3: 1.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 234.136827821
• Heavy Atom Count: 17
• Complexity: 271

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of N-[1-(aminocarbonyl)-3-methylbutyl]benzamide

There total 3 articles about N-[1-(aminocarbonyl)-3-methylbutyl]benzamide 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: 37.0%

(2-Benzoylamino-4-methyl-pentanoylamino)-acetic acid methyl ester → N-benzoyl-leucine amide (24250-71-3)

Guidance literature:

With nickel(IV) oxide; In benzene; for 4h; Heating;

DOI:10.1016/S0040-4020(97)00216-0

Reference yield:

N-benzoyl-leucyl chloride (861602-55-3) → N-benzoyl-leucine amide (24250-71-3)

Guidance literature:

With ammonia;

Reference yield:

→ N-benzoyl-leucine amide (24250-71-3)

Guidance literature:

(11), H2/Ni, aethanol. NH3;

DOI:10.1021/jo00983a034

upstream raw materials:

N-benzoyl-leucyl chloride