alpha-Mercapto-n-butyrophenon

Base Information

Chemical Name:alpha-Mercapto-n-butyrophenon
CAS No.:13714-87-9
Molecular Formula:C₁₀H₁₂OS
Molecular Weight:180.271
Hs Code.:
DSSTox Substance ID:DTXSID001305328

Synonyms:alpha-Mercapto-n-butyrophenon;SCHEMBL3810221;2-Mercapto-1-phenyl-1-butanone;DTXSID001305328;13714-87-9

Suppliers and Price of alpha-Mercapto-n-butyrophenon

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of alpha-Mercapto-n-butyrophenon

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:180.06088618
Heavy Atom Count:12
Complexity:150

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC(C(=O)C1=CC=CC=C1)S

Technology Process of alpha-Mercapto-n-butyrophenon

There total 3 articles about alpha-Mercapto-n-butyrophenon 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: 84.0%

: 14313-57-6,73908-29-9
α-Chlor-n-butyrophenon

: 13714-87-9
α-Mercapto-n-butyrophenon

Guidance literature:: With sodium hydrogensulfide; In methanol; diethyl ether; at -20 ℃; for 4h;
DOI:10.1007/BF00808632

Reference yield:

: 14229-71-1
5-ethyl-2,4-diphenyl-2-propyl-2,5-dihydro-thiazole

: 13714-87-9
α-Mercapto-n-butyrophenon

Guidance literature:: With hydrogenchloride; In 1,4-dioxane;
DOI:10.1007/BF00902605

Reference yield:

: 495-40-9
propiophenone

: 13714-87-9
α-Mercapto-n-butyrophenon

Guidance literature:: Multi-step reaction with 2 steps

1: SO₂Cl₂ / CCl₄

2: H₂S, NaOMe / methanol

With sulfuryl dichloride; hydrogen sulfide; sodium methylate; In methanol; tetrachloromethane;
DOI:10.1007/BF00902605