Anilazine

Base Information

• Chemical Name: Anilazine
• CAS No.: 101-05-3
• Molecular Formula: C9H5 Cl3 N4
• Molecular Weight: 275.524
• Hs Code.: 2933699015
• European Community (EC) Number: 202-910-5
• NSC Number: 3851
• UN Number: 3077,2588
• UNII: C6E8Y03ZJN
• DSSTox Substance ID: DTXSID9020089
• Nikkaji Number: J5.237J
• Wikipedia: Anilazine
• Wikidata: Q413886
• ChEMBL ID: CHEMBL464135
• Mol file: 101-05-3.mol

Synonyms:anilazine;dyrene

Chemical Property of Anilazine

Chemical Property:

• Appearance/Colour: white to light brown crystals or powder
• Vapor Pressure: 1.17E-08mmHg at 25°C
• Melting Point: 159 - 160ºC
• Refractive Index: 1.679
• Boiling Point: 460.4 °C at 760 mmHg
• PKA: 0.43±0.10(Predicted)
• Flash Point: 232.2 °C
• PSA: 50.70000
• Density: 1.611 g/cm³
• LogP: 3.64840
• Storage Temp.: 0-6°C
• Water Solubility.: 10mg/L(temperature not stated)
• XLogP3: 3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 273.957979
• Heavy Atom Count: 16
• Complexity: 221
• Transport DOT Label: Class 9

Purity/Quality:

98%,99%, ^*data from raw suppliers

Anilazine ^*data from reagent suppliers

Safty Information:

• Pictogram(s): XiN
• Hazard Codes: Xi,N
• Statements: 36/38-50/53
• Safety Statements: 22-60-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Fungicides
• Canonical SMILES: C1=CC=C(C(=C1)NC2=NC(=NC(=N2)Cl)Cl)Cl
• Uses: Pesticide used to control fungus diseases in lawns and turf. Fungicide. Nonsystemic, foliar fungicide used in potatoes, tomatoes, wheat, barley and ornamentals.

Technology Process of Anilazine

There total 17 articles about Anilazine 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: 79.0%

→ 2,4,6-Tris(1',1'-difluoro-3'-butenyl)-1,3,5-triazine (188258-95-9) + anilazine (101-05-3)

Guidance literature:

Reference yield: 75.0%

1,3,5-trichloro-2,4,6-triazine (108-77-0) + o-chloroaniline (95-51-2) → anilazine (101-05-3)

Guidance literature:

With sodium hydroxide; In acetone; at 0 - 5 ℃; for 3h;

Reference yield: 70.0%

teroxirone (2451-62-9,28825-96-9,240408-78-0) + 4-Hydroxybenzophenone (1137-42-4) → anilazine (101-05-3)

Guidance literature:

With triphenylphosphine; In chloroform;

upstream raw materials:

1,3,5-trichloro-2,4,6-triazine

o-chloroaniline

teroxirone

4-Hydroxybenzophenone

Downstream raw materials:

2-(2,4-dihydroxy-5-hexylphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine

4-[4-cycloheptylamino-6-(methyl-piperidin-4-yl-amino)-[1,3,5]triazin-2-ylamino]-phenol

fluconazole

2-Mesityl-4-(2-hydroxy-4-n-hexyloxy-phenyl)-6-[2-hydroxy-4-(11-hydroxy-undecyloxy)phenyl]-1,3,5-triazine

Refernces

• 1、 Lee, Taeho,Seo, Young Ho. "Targeting the hydrophobic region of Hsp90's ATP binding pocket with novel 1,3,5-triazines". supporting information. p. 6427 - 6431. Retrieved 2013/11/19.
• 2、 -. "Dyes and their use in ink-jet printing". . . Retrieved 2008/12/07.