Butocarboxime

Base Information

• Chemical Name: Butocarboxime
• CAS No.: 34681-10-2
• Molecular Formula: C7H14 N2 O2 S
• Molecular Weight: 190.266
• Hs Code.: 2930909051
• European Community (EC) Number: 252-139-3
• Nikkaji Number: J19.750E
• Wikipedia: Butocarboxim
• Wikidata: Q1017979
• NCI Thesaurus Code: C163634
• Metabolomics Workbench ID: 55877
• Mol file: 34681-10-2.mol

Synonyms:butocarboxime;Drawin

Chemical Property of Butocarboxime

Chemical Property:

• Vapor Pressure: 1.1×10-2pa(20°C)
• Melting Point: 37℃ (E isomer)
• Refractive Index: 1.5690 (estimate)
• Boiling Point: °Cat760mmHg
• PKA: 13.83±0.46(Predicted)
• Flash Point: °C
• PSA: 75.99000
• Density: 1.12g/cm³
• LogP: 1.86070
• Water Solubility.: 35,000 mg l-1 at 20℃
• XLogP3: 1.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 190.07759887
• Heavy Atom Count: 12
• Complexity: 182

Purity/Quality:

99.0% ^*data from raw suppliers

Butocarboxim ^*data from reagent suppliers

Safty Information:

• Hazard Codes: T,N
• Statements: 10-23/24/25-36-50/53
• Safety Statements: 36/37-45-60-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Carbamate Insecticides
• Canonical SMILES: CC(C(=NOC(=O)NC)C)SC
• Isomeric SMILES: CC(/C(=N\OC(=O)NC)/C)SC
• Uses: Butocarboxim is a systematic selectively acting insecticide with anticholinesterasic activity. Butocarboxim is used to control sucking pests such as mites, aphids, white flies as well as bees in agric ulture. Labelled Butocarboxim, a systematic selectively acting insecticide with anticholinesterasic activity. Butocarboxim is used to control sucking pests such as mites, aphids, white flies as well as bees i n agriculture.

Technology Process of Butocarboxime

There total 1 articles about Butocarboxime 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:

→ butocarboxim (34681-10-2)

Guidance literature:

Entspr. Chlorketon, CH3SH, H2NOH, CH3NCO;