2-FORMAMIDINO-2-PHENYLDIAZOACETAMIDE HYDROCHLORIDE

Base Information

• Chemical Name: 2-FORMAMIDINO-2-PHENYLDIAZOACETAMIDE HYDROCHLORIDE
• CAS No.: 6285-64-9
• Molecular Formula: C9H11 N5 O . Cl H
• Molecular Weight: 242.665
• Mol file: 6285-64-9.mol

Synonyms:Acetamide,2-amidino-2-phenylazo-, hydrochloride (6CI); Propanamide, 3-amino-3-imino-2-(phenylazo)-,monohydrochloride (9CI); NSC 10849

Chemical Property of 2-FORMAMIDINO-2-PHENYLDIAZOACETAMIDE HYDROCHLORIDE

Chemical Property:

• Vapor Pressure: 4.76E-05mmHg at 25°C
• Boiling Point: 349.2°C at 760 mmHg
• Flash Point: 165°C
• PSA: 117.68000
• Density: 1.4g/cm³
• LogP: 2.86250

Purity/Quality:

97% ^*data from raw suppliers

3-Amino-3-imino-2-(2-phenyldiazenyl)propanamideHydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: 3-Amino-3-imino-2-(2-phenyldiazenyl)propanamide Hydrochloride is a Temozolomide (T017775) impurity. Temozolomide acts as a imidazotetrazine alkylating agent. An antineoplastic.

Technology Process of 2-FORMAMIDINO-2-PHENYLDIAZOACETAMIDE HYDROCHLORIDE

There total 1 articles about 2-FORMAMIDINO-2-PHENYLDIAZOACETAMIDE 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:

benzene diazonium chloride (100-34-5) + malonamamidine hydrochloride (34570-17-7) → phenylazomalonamamidine hydrochloride (6285-64-9)

Guidance literature:

Reference yield: 100.0%

4-chlorobenzaldehyde (104-88-1) + phenylazomalonamamidine hydrochloride (6285-64-9) → 2,8-di(p-chlorophenyl)-hypoxanthine (81976-26-3)

Guidance literature:

at 170 ℃; for 1h;

DOI:10.1246/cl.1982.365

Reference yield: 100.0%

4-chlorobenzaldehyde (104-88-1) + phenylazomalonamamidine hydrochloride (6285-64-9) → 2-{N-[1-(4-Chloro-phenyl)-meth-(E)-ylidene]-carbamimidoyl}-2-phenylazo-acetamide; hydrochloride (81990-65-0)

Guidance literature:

at 120 ℃; for 0.25h;

DOI:10.1246/cl.1982.365

upstream raw materials:

benzene diazonium chloride

malonamamidine hydrochloride

Downstream raw materials:

2,8-Di-p-tolyl-1,7-dihydro-purin-6-one

2,8-di(p-chlorophenyl)-hypoxanthine

2-{N-[1-(4-Chloro-phenyl)-meth-(E)-ylidene]-carbamimidoyl}-2-phenylazo-acetamide; hydrochloride

2,8-diphenyl-1,7-dihydro-purin-6-one

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