propachlor-2-hydroxy

Base Information

• Chemical Name: propachlor-2-hydroxy
• CAS No.: 42404-06-8
• Molecular Formula: C11H15 N O2
• Molecular Weight: 193.24
• Hs Code.: 2924299090
• Mol file: 42404-06-8.mol

Synonyms:2-Hydroxy-N-isopropyl-N-phenylacetamide;2-Hydroxy-N-isopropylacetanilide; N-Isopropylglycolanilide

Chemical Property of propachlor-2-hydroxy

Chemical Property:

• Melting Point: 39 °C
• Boiling Point: 305.6±25.0 °C(Predicted)
• PKA: 13.02±0.10(Predicted)
• PSA: 40.54000
• Density: 1.123±0.06 g/cm3(Predicted)
• LogP: 1.42030

Purity/Quality:

99% ^*data from raw suppliers

PROPACHLOR-2-HYDROXY 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: Propachlor-2-hydroxy is a metabolite or photodegrdation product of propachlor herbicide.

Technology Process of propachlor-2-hydroxy

There total 2 articles about propachlor-2-hydroxy 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-N-(1-methylethyl)-N-phenylacetamide (1918-16-7) → hydroxy-N-isopropyl-N-phenyl-acetamide (42404-06-8)

Guidance literature:

With hydroxide; at 25 ℃; Kinetics;

DOI:10.1021/jf030290d

Reference yield:

→ hydroxy-N-isopropyl-N-phenyl-acetamide (42404-06-8)

Guidance literature:

Reference yield:

2-chloro-5-methyl-1,3-benzoxazole (3770-60-3) + hydroxy-N-isopropyl-N-phenyl-acetamide (42404-06-8) → 2-(5-methyl-benzoxazol-2-yl-oxy)-N-isopropyl-acetanilide

Guidance literature:

With sodium hydroxide; In water; acetone;

upstream raw materials:

2-chloro-N-(1-methylethyl)-N-phenylacetamide

Downstream raw materials:

5-(1-methyl-2-chloro-2,3,3-trifluoro-1-cyclobutyl)-1,3,4-thiadiazol-2-yl-oxyacetic acid-N-isopropyl-anilide

Refernces

• 1、 Lippa, Katrice A.,Demel, Sandra,Lau, Irvin H.,Roberts, A. Lynn. "Kinetics and Mechanism of the Nucleophilic Displacement Reactions of Chloroacetanilide Herbicides: Investigation of α-Substituent Effects". . p. 3010 - 3021. Retrieved 2007/10/03.
• 2、 -. "Phenyl alpha-acyloxyacetamide derivatives and their therapeutic use". . . Retrieved 2008/06/13.