Trichlamide

Base Information

• Chemical Name: Trichlamide
• CAS No.: 70193-21-4
• Molecular Formula: C13H16 Cl3 N O3
• Molecular Weight: 340.634
• Hs Code.: 29242990
• European Community (EC) Number: 804-173-0
• DSSTox Substance ID: DTXSID00867877
• Nikkaji Number: J364.596G
• Wikidata: Q27155714
• Mol file: 70193-21-4.mol

Synonyms:Trichlamide;70193-21-4;Hataclean;N-(1-Butoxy-2,2,2-trichloroethyl)-2-hydroxybenzamide;Trichlamide [ISO];NK 483;WL 105305;BRN 2882884;(RS)-N-(1-Butoxy-2,2,2-trichloroethyl)salicylamide;Benzamide, N-(1-butoxy-2,2,2-trichloroethyl)-2-hydroxy-;N-(l-Butoxy-2,2,2-trichloroethyl)salicylamide;Trichlamide 10 microg/mL in Cyclohexane;SCHEMBL70426;C13H16Cl3NO3;CHEBI:82058;DTXSID00867877;C13-H16-Cl3-N-O3;LS-25983;C18916;Trichlamide, PESTANAL(R), analytical standard;N-(1-Butoxy-2,2,2-trichloroethyl)salicylamide;Q27155714;2-BENZYLSULFANYL-7-HYDROXY-[1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE-6-CARBOXYLICACIDETHYLESTER

Chemical Property of Trichlamide

Chemical Property:

• Vapor Pressure: 5.52E-09mmHg at 25°C
• Melting Point: 71～73℃71.0～73.0℃
• Refractive Index: 1.6200 (estimate)
• Boiling Point: 457.4 °C at 760 mmHg
• Flash Point: 230.4 °C
• PSA: 58.56000
• Density: 1.353 g/cm³
• LogP: 4.02590
• Storage Temp.: 0-6°C
• XLogP3: 4.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 339.019576
• Heavy Atom Count: 20
• Complexity: 310

Purity/Quality:

98%Min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCOC(C(Cl)(Cl)Cl)NC(=O)C1=CC=CC=C1O
• Uses: Trichlamide is a fungicide used in crops and on produce. Pesticide.

Technology Process of Trichlamide

There total 1 articles about Trichlamide 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:

→ trichlamide (70193-21-4)

Guidance literature:

Verb. /BRN= 941358/, n-Butanol;

Refernces

• 1、 -. "Iminoacetic acid amides and their use as pest control agents". . . Retrieved 2008/06/13.
• 2、 -. "Halogen alkenyl azolyl microbicides". . . Retrieved 2008/06/13.