N²-[amino(selenocarbonyl)]-4-chloro-N¹-phenylbenzimidamide

Base Information

• Chemical Name: N²-[amino(selenocarbonyl)]-4-chloro-N¹-phenylbenzimidamide
• CAS No.: 294644-46-5
• Molecular Formula: C₁₄H₁₂ClN₃Se
• Molecular Weight: 336.682
• Mol file: 294644-46-5.mol

Synonyms:N²-[amino(selenocarbonyl)]-4-chloro-N¹-phenylbenzimidamide

Chemical Property of N²-[amino(selenocarbonyl)]-4-chloro-N¹-phenylbenzimidamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N²-[amino(selenocarbonyl)]-4-chloro-N¹-phenylbenzimidamide

There total 3 articles about N²-[amino(selenocarbonyl)]-4-chloro-N¹-phenylbenzimidamide 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: 75.0%

4-chloro-N-phenylbenzimidoyl isoselenocyanate → N2-[amino(selenocarbonyl)]-4-chloro-N1-phenylbenzimidamide (294644-46-5)

Guidance literature:

With ammonia; In acetone; at 25 ℃;

DOI:10.1002/1522-2675(20000705)83:7<1576::AID-HLCA1576>3.0.CO;2-M

Reference yield:

4-chlorobenzanilide (6833-15-4) → N2-[amino(selenocarbonyl)]-4-chloro-N1-phenylbenzimidamide (294644-46-5)

Guidance literature:

Multi-step reaction with 3 steps

1: SOCl₂ / 3 h / Heating

2: acetone

3: 75 percent / NH₃ / acetone / 25 °C

With thionyl chloride; ammonia; In acetone; 1: Substitution / 2: Substitution / 3: Addition;

DOI:10.1002/1522-2675(20000705)83:7<1576::AID-HLCA1576>3.0.CO;2-M

Reference yield:

N-Phenyl-4-chlor-benzimid-saeurechlorid (38430-13-6) → N2-[amino(selenocarbonyl)]-4-chloro-N1-phenylbenzimidamide (294644-46-5)

Guidance literature:

Multi-step reaction with 2 steps

1: acetone

2: 75 percent / NH₃ / acetone / 25 °C

With ammonia; In acetone; 1: Substitution / 2: Addition;

DOI:10.1002/1522-2675(20000705)83:7<1576::AID-HLCA1576>3.0.CO;2-M

upstream raw materials:

4-chlorobenzanilide

N-Phenyl-4-chlor-benzimid-saeurechlorid