Clemizole penicillin

Base Information

• Chemical Name: Clemizole penicillin
• CAS No.: 6011-39-8
• Molecular Formula: C35H38ClN5O4S
• Molecular Weight: 660.235
• UNII: 5UL276H6TF
• DSSTox Substance ID: DTXSID10975533
• Wikidata: Q27123267
• NCI Thesaurus Code: C80594
• Mol file: 6011-39-8.mol

Synonyms:clemizole penicillin G;clemizolpenicillin

Chemical Property of Clemizole penicillin

Chemical Property:

• Vapor Pressure: 2.29E-10mmHg at 25°C
• Melting Point: 144-145°
• Boiling Point: 506.1°C at 760 mmHg
• Flash Point: 259.9°C
• PSA: 145.35000
• LogP: 5.48730
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 8
• Exact Mass: 659.2333036
• Heavy Atom Count: 46
• Complexity: 907

Purity/Quality:

98%Min ^*data from raw suppliers

CLEMIZOLE PENICILLIN 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)O)C.C1CCN(C1)CC2=NC3=CC=CC=C3N2CC4=CC=C(C=C4)Cl
• Isomeric SMILES: CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CC=C3)C(=O)O)C.C1CCN(C1)CC2=NC3=CC=CC=C3N2CC4=CC=C(C=C4)Cl
• Uses: Neopenyl can be used to treat topical microbial infections.

Technology Process of Clemizole penicillin

There total 1 articles about Clemizole penicillin 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:

→ 3,3-Dimethyl-7-oxo-6-phenylacetylamino-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid; compound with 1-(4-chloro-benzyl)-2-pyrrolidin-1-ylmethyl-1H-benzoimidazole (6011-39-8,39539-51-0)

Guidance literature:

Thiazolin, O=C=CH-NH-Acyl.;