Promecarb

Base Information

• Chemical Name: Promecarb
• CAS No.: 2631-37-0
• Deprecated CAS: 31677-56-2,4111-89-1,4111-89-1
• Molecular Formula: C12H17 N O2
• Molecular Weight: 207.272
• Hs Code.: 2924199090
• European Community (EC) Number: 220-113-0
• NSC Number: 35378
• UN Number: 2757
• UNII: 1QRP20775S
• DSSTox Substance ID: DTXSID4037617
• Nikkaji Number: J3.034A
• Wikipedia: Promecarb
• Wikidata: Q7249684
• NCI Thesaurus Code: C163695
• ChEMBL ID: CHEMBL1076537
• Mol file: 2631-37-0.mol

Synonyms:3-cym-5-yl methylcarbamate;3-methyl-5-isopropylphenyl N-methylcarbamate;Carbamult;m-cym-5-yl methylcarbamate;promecarb

Chemical Property of Promecarb

Chemical Property:

• Melting Point: 87-88ºC
• Refractive Index: 1.5220 (estimate)
• Boiling Point: 282°Cat760mmHg
• PKA: 12.37±0.46(Predicted)
• Flash Point: 124.3°C
• PSA: 38.33000
• Density: 1.024g/cm³
• LogP: 3.22750
• Storage Temp.: 0-6°C
• Solubility.: Chloroform (Slightly), Methanol (Slightly)
• Water Solubility.: 92mg/L(room temperature)
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 207.125928785
• Heavy Atom Count: 15
• Complexity: 216
• Transport DOT Label: Poison

Purity/Quality:

99% ^*data from raw suppliers

Promecarb-d3 ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Toxic by ingestion.
• Hazard Codes: T,N
• Statements: 25-50/53
• Safety Statements: 24-37-45-60-61

MSDS Files:

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Carbamate Insecticides
• Canonical SMILES: CC1=CC(=CC(=C1)OC(=O)NC)C(C)C
• Uses: Insecticide. Promecarb is a carbamate pesticide.

Technology Process of Promecarb

There total 1 articles about Promecarb 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-methyl-5-i-propylphenyl N-methylcarbamate (2631-37-0)

Guidance literature:

Reference yield:

3-methyl-5-i-propylphenyl N-methylcarbamate (2631-37-0) → carbon dioxide (124-38-9,18923-20-1) + 3-isopropyl-5-methylphenol (3228-03-3) + methylamine (74-89-5)

Guidance literature:

With borate buffer; cetyltrimethylammonim bromide; In water; at 100 ℃; for 0.00833333h; pH=9.0; Further Variations:; Temperatures; Product distribution;

DOI:10.1021/ac990928d

Reference yield:

3-methyl-5-i-propylphenyl N-methylcarbamate (2631-37-0) → Sodium; 3-isopropyl-5-methyl-phenolate

Guidance literature:

With sodium hydroxide; In water;

Downstream raw materials:

carbon dioxide

3-isopropyl-5-methylphenol

methylamine

3-isopropyl-5-hydroxybenzaldehyde

Refernces

• 1、 -. "Propynyl benzyl ethers". . . Retrieved 2008/06/13.