Benzoyl chloride, 2-(2-propynyloxy)-

Base Information

Chemical Name:Benzoyl chloride, 2-(2-propynyloxy)-
CAS No.:65211-53-2
Molecular Formula:C10H7ClO2
Molecular Weight:194.617
Hs Code.:
DSSTox Substance ID:DTXSID10442715
Nikkaji Number:J1.121.937C
Wikidata:Q82260158

Synonyms:65211-53-2;Benzoyl chloride, 2-(2-propynyloxy)-;SCHEMBL16364110;DTXSID10442715;2-[(2-Propynyl)oxy]benzoyl chloride

Suppliers and Price of Benzoyl chloride, 2-(2-propynyloxy)-

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 1 raw suppliers

Chemical Property of Benzoyl chloride, 2-(2-propynyloxy)-

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:194.0134572
Heavy Atom Count:13
Complexity:228

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C#CCOC1=CC=CC=C1C(=O)Cl

Technology Process of Benzoyl chloride, 2-(2-propynyloxy)-

There total 4 articles about Benzoyl chloride, 2-(2-propynyloxy)- 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:

: 55582-31-5
2-(prop-2-yn-1-yloxy)benzoic acid

: 65211-53-2
2-Prop-2-ynyloxybenzoic acid chloride

Guidance literature:: With oxalyl dichloride;
DOI:10.1021/ja00099a011

Reference yield:

: 59155-84-9
methyl 2-(prop-2-yn-1-yloxy)benzoate

: 65211-53-2
2-Prop-2-ynyloxybenzoic acid chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / H₂O, KOH / ethanol / 25 h / Ambient temperature

2: SOCl₂ / 0.5 h / Heating

With potassium hydroxide; thionyl chloride; water; In ethanol;

Reference yield:

: 119-36-8,8024-54-2
methyl salicylate

: 65211-53-2
2-Prop-2-ynyloxybenzoic acid chloride

Guidance literature:: Multi-step reaction with 3 steps

1: 74 percent / K₂CO₃ / acetone; toluene / 24 h / Heating

2: 73 percent / H₂O, KOH / ethanol / 25 h / Ambient temperature

3: SOCl₂ / 0.5 h / Heating

With potassium hydroxide; thionyl chloride; water; potassium carbonate; In ethanol; acetone; toluene;