Mesocarb

Base Information

• Chemical Name: Mesocarb
• CAS No.: 34262-84-5
• Molecular Formula: C18H18 N4 O2
• Molecular Weight: 322.366
• UNII: UMT8MP2NDU
• DSSTox Substance ID: DTXSID10900961
• Wikipedia: Mesocarb
• NCI Thesaurus Code: C83937
• ChEMBL ID: CHEMBL3989800,CHEMBL2105246
• Mol file: 34262-84-5.mol

Synonyms:mesocarb;N-phenylcarbamoyl-3-(beta-phenylisopropyl)sydnonimine;sidnocarb;sydnocarb

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Chemical Property of Mesocarb

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 75.91000
• Density: g/cm³
• LogP: 3.42620
• XLogP3: 4.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 322.14297583
• Heavy Atom Count: 24
• Complexity: 406

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(CC1=CC=CC=C1)[N+]2=NOC(=C2)N=C(NC3=CC=CC=C3)[O-]
• Isomeric SMILES: CC(CC1=CC=CC=C1)[N+]2=NOC(=C2)/N=C(/NC3=CC=CC=C3)\[O-]
• Uses: Mesocarb is a CNS stimulant that acts as a dopamine reuptake inhibitor. Mesocarb is a psychotropic drug. Mesocarb is used to counteract the sedative effects of benzodiazepine drugs.

Refernces

SYNTHESIS AND ANTIMONOAMINE OXIDASE ACTIVITY OF INKASAN AND ANALOGS OF IT

10.1007/BF00765589

The research focuses on the synthesis and study of biological properties of certain chemical compounds. One part of the research involves the synthesis and pharmacological investigation of analogs of sydnocarb and inkasan. The compounds synthesized include those with hydrophobic and hydrophilic properties, and their central stimulant activity is studied. The chemicals involved in this part of the research include sydnocarb, compounds (I, II, III), N,N-dialkylaminoethyl substituted β-carbolines (IIa, b), azepino[3,4-b]indole (V), and dichlorophosphonates (VI). Another part of the research involves the synthesis of new derivatives of 5-carboxymethylthiazolidine-2,4-dione and thiocarbohydrazide. The main starting materials for this synthesis are thiosemicarbazones of 4-alkoxybenzaldehydes and 4-alkoxyacetophenones. The chemicals involved in this part of the research include maleic anhydride, thiosemicarbazide, and thiocarbohydrazide.