N-Phenylbenzenecarboximidohydrazide

Base Information

• Chemical Name: N-Phenylbenzenecarboximidohydrazide
• CAS No.: 2038-98-4
• Molecular Formula: C13H13N3
• Molecular Weight: 211.266
• DSSTox Substance ID: DTXSID80596754
• Wikidata: Q82492089
• Mol file: 2038-98-4.mol

Synonyms:N-Phenylbenzenecarboximidohydrazide;2038-98-4;benzimidic acid phenyl hydrazide;SCHEMBL4105515;DTXSID80596754;UUOVEMDVDIRIJV-UHFFFAOYSA-N

Chemical Property of N-Phenylbenzenecarboximidohydrazide

Chemical Property:

• XLogP3: 2.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 211.110947427
• Heavy Atom Count: 16
• Complexity: 227

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(=N)N(C2=CC=CC=C2)N

Technology Process of N-Phenylbenzenecarboximidohydrazide

There total 4 articles about N-Phenylbenzenecarboximidohydrazide 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:

N-phenyl benzoyl amide (93-98-1,5705-51-1) → N-phenylbenzamidrazone (2038-98-4)

Guidance literature:

With thionyl chloride; hydrazine; Yield given. Multistep reaction; 1.) reflux, 18 h, 2) C₆H₆, RT, 18 h;

DOI:10.1021/jm00097a007

Reference yield:

N-phenyl-benzimidoyl chloride (4903-36-0) → N''-phenyl-benzamidrazone (2038-98-4)

Guidance literature:

With Petroleum ether; hydrazine;

Reference yield:

→ N-phenylbenzamidrazone (2038-98-4)

Guidance literature:

Thiobenzanilid, Hydrazinhydrat;

DOI:10.1055/s-1979-28680

upstream raw materials:

N-phenyl benzoyl amide

N-phenyl-benzimidoyl chloride

Downstream raw materials:

3,4,5-triphenyl-1,2,4-triazole

C₁₄H₁₄N₄S

3,4,8,9-Tetraphenyl-1,2,4,6,7,9-hexaaza-5λ⁵-phospha-spiro[4.4]nona-2,7-diene

1,2,4,5,7,8,10,11-Octaphenyl-1H,4H,7H,10H-1,3,3a,4,6,6a,7,9,9a,10,12,12a-dodecaaza-3b,6b,9b,12b-tetraphospha-tetracyclopenta[a,c,e,g]cyclooctene

Refernces