4-Allyloxybenzoyl chloride

Base Information

Chemical Name:4-Allyloxybenzoyl chloride
CAS No.:36844-51-6
Molecular Formula:C10H9 Cl O2
Molecular Weight:196.633
Hs Code.:29189990
DSSTox Substance ID:DTXSID00472824
Nikkaji Number:J1.091.552J
Wikidata:Q82301990
Mol file:36844-51-6.mol

Synonyms:4-ALLYLOXYBENZOYL CHLORIDE;36844-51-6;4-prop-2-enoxybenzoyl Chloride;p-allyloxybenzoyl chloride;4-allyloxy benzoyl chloride;4-(Allyloxy)benzoyl chloride;SCHEMBL711175;DTXSID00472824;WYMVIVUKHYHNBN-UHFFFAOYSA-N;4-(2-propenyloxy)benzoyl chloride;MFCD09744024;4-(prop-2-en-1-oxy)benzoyl chloride;AKOS030220496;4-(allyloxy)-1-benzenecarbonyl chloride

Suppliers and Price of 4-Allyloxybenzoyl chloride

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

Atlantic Research Chemicals
4-(Allyloxy)benzoylchloride 95%
1gm:
$ 356.99

Total 4 raw suppliers

Chemical Property of 4-Allyloxybenzoyl chloride

Chemical Property:

PSA：26.30000
LogP:2.63040
Storage Temp.:Freezer (-20°C)
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:196.0291072
Heavy Atom Count:13
Complexity:183

Purity/Quality:

99% ^*data from raw suppliers

4-(Allyloxy)benzoylchloride 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CCOC1=CC=C(C=C1)C(=O)Cl

Technology Process of 4-Allyloxybenzoyl chloride

There total 6 articles about 4-Allyloxybenzoyl chloride 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%

: 27914-60-9
4-allyloxybenzoic acid

: 36844-51-6
4-allyloxybenzoyl chloride

Guidance literature:: With thionyl chloride; at 20 - 55 ℃; for 7h;
DOI:10.1021/acs.macromol.5b00101

Reference yield:

: 99-96-7
4-hydroxy-benzoic acid

: 36844-51-6
4-allyloxybenzoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: KOH / methanol / 1 h / Heating

2: SOCl₂ / dimethylformamide / Heating

With potassium hydroxide; thionyl chloride; In methanol; N,N-dimethyl-formamide;
DOI:10.1021/np049873n

Reference yield:

: 99-96-7
4-hydroxy-benzoic acid

: 36844-51-6
4-allyloxybenzoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / KOH; NaI / ethanol / 20 h / Heating

2: 91 percent / (COCl)2 / CH₂Cl₂ / 3 h / 20 °C

With potassium hydroxide; oxalyl dichloride; sodium iodide; In ethanol; dichloromethane;
DOI:10.1021/jm030086h