2,4-Dichloro-5-isopropoxyaniline

Base Information

• Chemical Name: 2,4-Dichloro-5-isopropoxyaniline
• CAS No.: 41200-96-8
• Molecular Formula: C9H11 Cl2 N O
• Molecular Weight: 220.098
• Hs Code.: 2922299090
• European Community (EC) Number: 255-258-9
• UNII: HTL4BZ5C7X
• DSSTox Substance ID: DTXSID90194124
• Nikkaji Number: J28.397E
• Wikidata: Q83066878
• ChEMBL ID: CHEMBL1892783
• Mol file: 41200-96-8.mol

Synonyms:2,4-Dichloro-5-isopropoxyaniline;41200-96-8;2,4-dichloro-5-propan-2-yloxyaniline;2,4-Dichloro-5-isopropyloxyaniline;HTL4BZ5C7X;Benzenamine, 2,4-dichloro-5-(1-methylethoxy)-;2,4-Dichloro-5-(2-propyloxy)aniline;2,4-dichloro-5-(propan-2-yloxy)aniline;EINECS 255-258-9;EC 255-258-9;2,4-dichloro-5-isopropoxyphenylamine;UNII-HTL4BZ5C7X;Bionet2_001044;Oprea1_658657;MLS000707238;SCHEMBL3277991;CHEMBL1892783;DTXSID90194124;HMS1366P10;HMS2660J22;2,4-dichloro-5-isopropoxy-aniline;MFCD00974411;AKOS015992780;4L-351S;SB79605;2,4-dichloro-5-(1-methylethoxy)aniline;NCGC00246545-01;SMR000334623;CS-0274551;FT-0610013;EN300-1154107;A825461;2,4-DICHLORO-5-(1-METHYLETHOXY)BENZENAMINE

Chemical Property of 2,4-Dichloro-5-isopropoxyaniline

Chemical Property:

• Vapor Pressure: 0.000585mmHg at 25°C
• Melting Point: 40-42°C
• Boiling Point: 110-112°C 0,2mm
• Flash Point: 141.8°C
• PSA: 35.25000
• Density: 1.272g/cm³
• LogP: 3.94400
• XLogP3: 3.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 219.0217694
• Heavy Atom Count: 13
• Complexity: 166

Purity/Quality:

99.9% ^*data from raw suppliers

2,4-Dichloro-5-isopropoxyaniline 97% ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 20/21/22
• Safety Statements: 28-36/37

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)OC1=C(C=C(C(=C1)N)Cl)Cl

Technology Process of 2,4-Dichloro-5-isopropoxyaniline

There total 7 articles about 2,4-Dichloro-5-isopropoxyaniline 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: 98.0%

N-[2,4-dichloro-5-(propan-2-yloxy)phenyl]acetamide (65948-71-2) → 2,4-dichloro-5-isopropoxyaniline (41200-96-8)

Guidance literature:

With sodium hydroxide; In ethanol; water; for 8h; Time;

Reference yield:

2,4-dichloro-5-isopropoxy-1-nitrobenzene (41200-97-9) → 2,4-dichloro-5-isopropoxyaniline (41200-96-8)

Guidance literature:

With hydrogen;

Reference yield:

2,4-dichloro-5-(1-methylethoxy) acetanilide → 2,4-dichloro-5-isopropoxyaniline (41200-96-8)

Guidance literature:

With hydrogenchloride; sodium carbonate; In water;

upstream raw materials:

2,4-dichloro-5-isopropoxy-1-nitrobenzene

2,4-dichloro-5-nitrophenol?

m-Hydroxyaniline

meta-hydroxyacetanilide

Downstream raw materials:

2,4-dichloro-5-(1-methylethoxy)phenylhydrazine

E-2-[2,4-Dichloro-5(1-methylethoxy)phenyl]-1,2,4-triazine-3,5(2H,4H)dione-6-carboxylic acid

2-(2,4-dichloro-5-isopropoxyphenyl)-1,2,4,5,6,7-hexahydro-3H-indazol-3-one

Refernces

• 1、 -. "Oxadiazon synthesis method". Paragraph 0018; 0038. . Retrieved 2017/06/02.
• 2、 -. "Herbicidal 2-aryl-1,2,4-triazine-3,5(2H,4H)-diones and sulfur analogs thereof". . . Retrieved 2008/06/13.