2,3,5-Trimethylphenyl methylcarbamate

Base Information

• Chemical Name: 2,3,5-Trimethylphenyl methylcarbamate
• CAS No.: 2655-15-4
• Deprecated CAS: 58784-13-7
• Molecular Formula: C11H15 N O2
• Molecular Weight: 193.246
• Hs Code.: 2924199090
• European Community (EC) Number: 602-974-8,684-207-7
• UN Number: 2811
• UNII: KQN4BOS2C6
• DSSTox Substance ID: DTXSID9041318
• Nikkaji Number: J67.103G
• Wikidata: Q27118022
• NCI Thesaurus Code: C163713
• Metabolomics Workbench ID: 56060
• Mol file: 2655-15-4.mol

Synonyms:Landrin;Landrin, (2,3,5)-isomer (landrin B);Landrin, (3,4,5)-isomer (landrina);trimethacarb;trimethylphenyl-N-methylcarbamate

Chemical Property of 2,3,5-Trimethylphenyl methylcarbamate

Chemical Property:

• Melting Point: 123-124 °C(Solv: methanol (67-56-1); ethanol (64-17-5); octane (111-65-9))
• Boiling Point: 287.8°Cat760mmHg
• PKA: 12.39±0.46(Predicted)
• Flash Point: 127.9°C
• PSA: 38.33000
• Density: 1.046g/cm³
• LogP: 2.72090
• Storage Temp.: 0-6°C
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 193.110278721
• Heavy Atom Count: 14
• Complexity: 206
• Transport DOT Label: Poison

Purity/Quality:

98%min ^*data from raw suppliers

2,3,5-Trimethacarb ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xn
• Statements: 22-36
• Safety Statements: 26

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Pesticides -> Carbamate Insecticides
• Canonical SMILES: CC1=CC(=C(C(=C1)OC(=O)NC)C)C

Technology Process of 2,3,5-Trimethylphenyl methylcarbamate

There total 2 articles about 2,3,5-Trimethylphenyl methylcarbamate 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:

2,3,5-trimethylphenol (697-82-5) + methyl isocyanate (624-83-9) → 2,3,5-trimethacarb (2655-15-4)

Guidance literature:

With di-isopropyl ether;

DOI:10.1021/jf60037a003

Reference yield:

→ 2,3,5-trimethacarb (2655-15-4)

Guidance literature:

entspr. Phenol, CH3NCO;

DOI:10.1021/jf60139a007

upstream raw materials:

2,3,5-trimethylphenol

methyl isocyanate