Diethatyl

Base Information

Chemical Name:Diethatyl
CAS No.:38725-95-0
Molecular Formula:C14H18 Cl N O3
Molecular Weight:283.755
Hs Code.:2924299090
UNII:JL34LTZ963
DSSTox Substance ID:DTXSID80192018
Nikkaji Number:J20.672E
Wikidata:Q22807422
Mol file:38725-95-0.mol

Synonyms:Diethatyl;38725-95-0;Diethatyl [ANSI:BSI:ISO];N-(Chloroacetyl)-N-(2,6-diethylphenyl)glycine;2-(N-(2-chloroacetyl)-2,6-diethylanilino)acetic acid;BRN 2871790;UNII-JL34LTZ963;JL34LTZ963;2-[(2-CHLOROACETYL)-(2,6-DIETHYLPHENYL)AMINO]ACETIC ACID;Glycine, N-(chloroacetyl)-N-(2,6-diethylphenyl)-;DIETHATYL [ISO];SCHEMBL131683;DTXSID80192018;LS-72375;N-CHLOROACETYL-N-(2,6-DIETHYLPHENYL)GLYCINE;Glycine, N-(2-chloroacetyl)-N-(2,6-diethylphenyl)-;Q22807422;Glycine, N-(chloroacetyl)-N-(2,6-diethylphenyl)- (9CI)

Suppliers and Price of Diethatyl

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 4 raw suppliers

Chemical Property of Diethatyl

Chemical Property:

Vapor Pressure:2.21E-10mmHg at 25°C
Boiling Point:489.2°Cat760mmHg
Flash Point:249.6°C
PSA：57.61000
Density:1.237g/cm³
LogP:2.46780
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:283.0975211
Heavy Atom Count:19
Complexity:310

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1=C(C(=CC=C1)CC)N(CC(=O)O)C(=O)CCl
Uses Diethatyl is used for selective, pre-emergence control of grass and broadleaved weeds. Diethatyl is a Preemergent herbicide for weed control.

Technology Process of Diethatyl

There total 4 articles about Diethatyl 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: 84.0%

: 79-04-9
chloroacetyl chloride

: 247056-42-4
2-(2,6-diethyl)anilinoethanoic acid

: 38725-95-0
N-chloroacetyl-N-(2,6-diethylphenyl)glycine

Guidance literature:: In dichloromethane; at 20 ℃; for 2h;
DOI:10.1021/jf990087b

Reference yield:

: 579-66-8
2,6-diethylaniline

: 38725-95-0
N-chloroacetyl-N-(2,6-diethylphenyl)glycine

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / Na₂CO₃ / 4 h / 140 °C

2: 80 percent / aq. NaOH / acetone / 14 h / 20 °C

3: 84 percent / CH₂Cl₂ / 2 h / 20 °C

With sodium hydroxide; sodium carbonate; In dichloromethane; acetone; 1: Alkylation / 2: Hydrolysis / 3: Acylation;
DOI:10.1021/jf990087b

Reference yield:

: 38727-56-9
2,6-diethyl-anilino-acetic acid ethyl ester

: 38725-95-0
N-chloroacetyl-N-(2,6-diethylphenyl)glycine

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / aq. NaOH / acetone / 14 h / 20 °C

2: 84 percent / CH₂Cl₂ / 2 h / 20 °C

With sodium hydroxide; In dichloromethane; acetone; 1: Hydrolysis / 2: Acylation;
DOI:10.1021/jf990087b