Metolachlor deschloro

Base Information

• Chemical Name: Metolachlor deschloro
• CAS No.: 126605-22-9
• Molecular Formula: C₁₅H₂₃NO₂
• Molecular Weight: 249.353
• DSSTox Substance ID: DTXSID901017794
• Nikkaji Number: J1.520.548B
• Mol file: 126605-22-9.mol

Synonyms:Metolachlor deschloro;126605-22-9;N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide;Metolachlor deschloro 100 microg/mL in Acetonitrile;Dechlorometolachlor;SCHEMBL6545091;DTXSID901017794;NS00040816;N-(2-ethyl-6-methylphenyl)-N-(methoxyprop-2-yl)acetamide;Acetamide, N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)-;N-(2-Ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)acetamide;Dechlorometolachlor, Acetamide, N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)-

Chemical Property of Metolachlor deschloro

Chemical Property:

• Boiling Point: 368.7±37.0 °C(Predicted)
• PKA: 1.63±0.50(Predicted)
• PSA: 29.54000
• Density: 1.011±0.06 g/cm3(Predicted)
• LogP: 2.94520
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 249.172878976
• Heavy Atom Count: 18
• Complexity: 267

Purity/Quality:

97% ^*data from raw suppliers

METOLACHLOR DESCHLORO 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC1=CC=CC(=C1N(C(C)COC)C(=O)C)C

Technology Process of Metolachlor deschloro

There total 1 articles about Metolachlor deschloro 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-chloro-6'-ethyl-N-(2-methoxy-1-methylethyl)acet-o-toluidide (51218-45-2) → N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide (126605-22-9)

Guidance literature:

With hydrogen; triethylamine; palladium on activated charcoal; In methanol;

DOI:10.1016/0040-4020(95)00556-N

Reference yield:

N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide (126605-22-9) → N-ethyl,N-(methoxyprop-2-yl),2-ethyl-6-methyl,aniline

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran;

DOI:10.1016/0040-4020(95)00556-N

Reference yield:

N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide (126605-22-9) → 3-(2-ethyl-6-methylphenyl)-2-hydroxy-4-methyl-2-methyloxazolidine

Guidance literature:

With hydrogenchloride; In methanol; at 79.9 ℃; Kinetics; Mechanism; Thermodynamic data; ΔF(excit.), ΔH(excit.), ΔS(excit.); various reagent concentrations, other reagent;

DOI:10.1016/0040-4020(95)00556-N

upstream raw materials:

2-chloro-6'-ethyl-N-(2-methoxy-1-methylethyl)acet-o-toluidide

Refernces

• 1、 Eykholt, Gerald R.,Davenport, Douglas T.. "Dechlorination of the chloroacetanilide herbicides alachlor and metolachlor by iron metal". . p. 1482 - 1487. Retrieved 1998.