2-Aminoacetanilide hydrochloride

Base Information

• Chemical Name: 2-Aminoacetanilide hydrochloride
• CAS No.: 4801-39-2
• Molecular Formula: C8H11ClN2O
• Molecular Weight: 186.641
• European Community (EC) Number: 817-104-4
• NSC Number: 14288
• UNII: 542J36T8CG
• Wikidata: Q27896870
• ChEMBL ID: CHEMBL1967357
• Mol file: 4801-39-2.mol

Synonyms:4801-39-2;2-amino-N-phenylacetamide hydrochloride;2-AMINOACETANILIDE HYDROCHLORIDE;Glycinanilide, hydrochloride;N1-phenylglycinamide hydrochloride;2-amino-N-phenylacetamide;hydrochloride;Acetamide, 2-amino-N-phenyl-, monohydrochloride;CCRIS 4573;2-Aminoacetanilide monohydrochloride;NSC 14288;Acetanilide, 2-amino-, monohydrochloride;2-Amino-N-phenylacetamide monohydrochloride;2-Amino-N-phenylacetamide HCl;542J36T8CG;NSC-14288;2-AMINOACETANILIDEHYDROCHLORIDE;NSC14288;2-amino-N-phenyl-acetamide;SCHEMBL355185;UNII-542J36T8CG;CHEMBL1967357;MFCD00035439;2-amino-N-phenylacetamidehydrochloride;AKOS015847712;AB22066;LS-1287;FT-0681534;EN300-48607;Q27896870;Acetamide, 2-amino-N-phenyl-, monohydrochloride (9CI);F3359-0054;Z594413794;ACETAMIDE, 2-AMINO-N-PHENYL-, HYDROCHLORIDE (1:1)

Chemical Property of 2-Aminoacetanilide hydrochloride

Chemical Property:

• Vapor Pressure: 2.06E-05mmHg at 25°C
• Boiling Point: 361.5°C at 760 mmHg
• Flash Point: 172.4°C
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 186.0559907
• Heavy Atom Count: 12
• Complexity: 130

Purity/Quality:

98%min ^*data from raw suppliers

2-Amino-N-phenylacetamidehydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)NC(=O)CN.Cl

Technology Process of 2-Aminoacetanilide hydrochloride

There total 9 articles about 2-Aminoacetanilide 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: 99.0%

→ 2-amino-N-phenylacetamide hydrochloride (4801-39-2)

Guidance literature:

Reference yield: 87.0%

benzyl (2-oxo-2-(phenylamino)ethyl)carbamate (6833-09-6) → 2-amino-N-phenylacetamide hydrochloride (4801-39-2)

Guidance literature:

With hydrogenchloride; hydrogen; palladium; In methanol;

Reference yield: 86.0%

N-glycyl>aniline (27904-92-3) → 2-amino-N-phenylacetamide hydrochloride (4801-39-2)

Guidance literature:

With hydrogenchloride; acetic acid; at 25 ℃; for 0.5h;

DOI:10.1021/jo00376a057

upstream raw materials:

hydroxyimino-N-phenylacetamide

benzyl (2-oxo-2-(phenylamino)ethyl)carbamate

N-glycyl>aniline

aniline

Downstream raw materials:

2-phenyl-[1,2,5]thiadiazol-3-one

N-alanyl-glycine anilide

(Z)-7-{(1S,2R,3R,4R)-3-[(Phenylcarbamoylmethyl-amino)-methyl]-7-oxa-bicyclo[2.2.1]hept-2-yl}-hept-5-enoic acid methyl ester

PhCH₂O-DL-Ala-Gly-NHPh