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2'-Mercaptovalerophenone

Base Information
  • Chemical Name:2'-Mercaptovalerophenone
  • CAS No.:870482-30-7
  • Molecular Formula:C11H14OS
  • Molecular Weight:194.298
  • Hs Code.:
  • DSSTox Substance ID:DTXSID801302142
  • Nikkaji Number:J2.569.456B
2'-Mercaptovalerophenone

Synonyms:2'-Mercaptovalerophenone;870482-30-7;DTXSID801302142;1-(2-Mercaptophenyl)-1-pentanone

Suppliers and Price of 2'-Mercaptovalerophenone
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Chemical Property of 2'-Mercaptovalerophenone
Chemical Property:
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:194.07653624
  • Heavy Atom Count:13
  • Complexity:168
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCCCC(=O)C1=CC=CC=C1S
Technology Process of 2'-Mercaptovalerophenone

There total 1 articles about 2'-Mercaptovalerophenone 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:
Guidance literature:
Thiosalicylic acid; With lithium hydride; In tetrahydrofuran; for 0.5h; Heating;
n-butyllithium; In tetrahydrofuran; diethyl ether; at 20 ℃; for 4h;
DOI:10.1080/10426500590912259
Guidance literature:
1-(2-sulfanylphenyl)pentan-1-one; With sodium hydride; In tetrahydrofuran; at 0 ℃; for 0.25h;
α-bromoacetophenone; In tetrahydrofuran; at 0 ℃; for 0.5h;
With sodium hydride; In tetrahydrofuran; at 0 ℃; for 0.5h; Further stages.;
DOI:10.3987/COM-07-11262
Guidance literature:
With (R)-3,3'-bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate; Ru2(OAc)4; In dichloromethane; at 0 ℃; for 7h; stereoselective reaction; Molecular sieve; Inert atmosphere;
DOI:10.1021/acs.orglett.8b01833
upstream raw materials:

n-butyllithium

Thiosalicylic acid

Downstream raw materials:

(3-butylbenzo[b]thiophen-2-yl)(phenyl)methanone

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