2-(Ethylthio)benzoyl chloride

Base Information

Chemical Name:2-(Ethylthio)benzoyl chloride
CAS No.:173312-15-7
Molecular Formula:C9H9ClOS
Molecular Weight:200.689
Hs Code.:
DSSTox Substance ID:DTXSID10564729
Wikidata:Q82449541

Synonyms:2-(ethylthio)benzoyl chloride;173312-15-7;2-ethylsulfanylbenzoyl chloride;2-(ethylsulfanyl)benzoyl chloride;2-(ethylthio)benzoylchloride;SCHEMBL2747139;DTXSID10564729;PRFYPNGSTNJXQV-UHFFFAOYSA-N;2-ethylsulfanylbenzoic acid chloride;AKOS015957753;EN300-237125;F2146-0429

Suppliers and Price of 2-(Ethylthio)benzoyl 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

Total 2 raw suppliers

Chemical Property of 2-(Ethylthio)benzoyl chloride

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:200.0062638
Heavy Atom Count:12
Complexity:161

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCSC1=CC=CC=C1C(=O)Cl

Technology Process of 2-(Ethylthio)benzoyl chloride

There total 4 articles about 2-(Ethylthio)benzoyl 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:

: 21101-79-1
2-ethylsulfanylbenzoic acid

: 173312-15-7
2-ethylsulfanyl benzoic acid chloride

Guidance literature:: With phosphorus pentachloride;
DOI:10.1021/ja01858a063

Reference yield:

: 118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4
anthranilic acid

: 173312-15-7
2-ethylsulfanyl benzoic acid chloride

Guidance literature:: Multi-step reaction with 2 steps

1: sodium nitrite; aqueous hydrochloric acid / Reaktion ueber mehrere Stufen

2: phosphorus (V)-chloride

With hydrogenchloride; phosphorus pentachloride; sodium nitrite;
DOI:10.1021/ja01858a063

Reference yield:

: 147-93-3
Thiosalicylic acid

: 173312-15-7
2-ethylsulfanyl benzoic acid chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / NaOH / methanol / 2 h

2: SOCl₂

With sodium hydroxide; thionyl chloride; In methanol;