3-Acetyloxy-4,4,4-trichlorobutanoic acid

Base Information

Chemical Name:3-Acetyloxy-4,4,4-trichlorobutanoic acid
CAS No.:6625-02-1
Molecular Formula:C₆H₇Cl₃O₄
Molecular Weight:249.478
Hs Code.:
NSC Number:53873
DSSTox Substance ID:DTXSID50288033

Synonyms:6625-02-1;NSC53873;ST023655;DTXSID50288033;NSC-53873;AKOS024278609

Suppliers and Price of 3-Acetyloxy-4,4,4-trichlorobutanoic acid

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 2 raw suppliers

Chemical Property of 3-Acetyloxy-4,4,4-trichlorobutanoic acid

Chemical Property:

Vapor Pressure:5.93E-07mmHg at 25°C
Boiling Point:383.8°Cat760mmHg
Flash Point:185.9°C
Density:1.556g/cm³
XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:247.940992
Heavy Atom Count:13
Complexity:210

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OC(CC(=O)O)C(Cl)(Cl)Cl

Technology Process of 3-Acetyloxy-4,4,4-trichlorobutanoic acid

There total 6 articles about 3-Acetyloxy-4,4,4-trichlorobutanoic acid 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:

: 90464-12-3
Acetic acid (E)-1-trichloromethyl-hept-3-enyl ester

: 6625-02-1
3-acetoxy-4,4,4-trichloro-butyric acid

Guidance literature:: With ruthenium tetroxide; In acetone;

Reference yield:

: 90701-62-5
1,1,1-trichloro-3-<(1S,5S)-6,6-dimethylbicyclo<3.3.1>hept-2-en-2-yl>propan-2-yl acetate

: 6625-02-1
(-)-γ,γ,γ-Trichlor-β-acetoxybuttersaeure

Guidance literature:: Multi-step reaction with 2 steps

1: 85percent m-chloroperbenzoic acid / CH₂Cl₂ / 36 h

2: 1.) 1M HCl, 2.) pyridinium chlorochromate, 3.) RuO₄

With hydrogenchloride; ruthenium tetroxide; 3-chloro-benzenecarboperoxoic acid; pyridinium chlorochromate; In dichloromethane;

Reference yield:

: 90701-62-5
1,1,1-trichloro-3-<(1S,5S)-6,6-dimethylbicyclo<3.1.1>hept-2-en-2-yl>propan-2-yl acetate

: 6625-02-1
(-)-γ,γ,γ-Trichlor-β-acetoxybuttersaeure

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / 85percent m-chloroperbenzoic acid / CH₂Cl₂ / 36 h

2: 1.) 1M HCl, 2.) pyridinium chlorochromate, 3.) RuO₄

With hydrogenchloride; ruthenium tetroxide; 3-chloro-benzenecarboperoxoic acid; pyridinium chlorochromate; In dichloromethane;