Home Indole and Oxindoles 480-94-4
480-94-4,MFCD20040182
Catalog No.:AA00I8O7

480-94-4 | 3-Mercaptoindole

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100mg
98%
in stock  
$45.00   $32.00
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250mg
98%
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$70.00   $49.00
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1g
98%
in stock  
$197.00   $138.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00I8O7
Chemical Name:
3-Mercaptoindole
CAS Number:
480-94-4
Molecular Formula:
C8H7NS
Molecular Weight:
149.2129
MDL Number:
MFCD20040182
SMILES:
Sc1c[nH]c2c1cccc2
Properties
Properties
 
BP:
326.6°C at 760 mmHg  
Form:
Solid  
MP:
99-100°C   
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
126  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
2  
XLogP3:
2.8  

Downstream Synthesis Route

[1]Zelesko,MichaelJ.;McComsey,DavidF.;Hageman,WilliamE.;Nortey,SamuelO.;Baker,CarolA.;Maryanoff,BruceE.[JournalofMedicinalChemistry,1983,vol.26,#2,p.230-237]

[1]Gurevich,P.A.;Komina,T.V.;Klimentova,G.Yu.;Zykova,T.V.;Ruzal',G.I.[PharmaceuticalChemistryJournal,1984,vol.18,#7,p.489-490][Khimiko-FarmatsevticheskiiZhurnal,1984,vol.18,#7,p.833-835]

[2]Gurevich,P.A.;Razumov,A.I.;Komina,T.V.;Klimentova,G.Yu.;Zykova,T.V.[JournalofgeneralchemistryoftheUSSR,1985,vol.55,#6,p.1187-1190][ZhurnalObshcheiKhimii,1985,vol.55,#6,p.1327-1331]

[1]Gurevich,P.A.;Razumov,A.I.;Komina,T.V.;Klimentova,G.Yu.;Zykova,T.V.[JournalofgeneralchemistryoftheUSSR,1985,vol.55,#6,p.1187-1190][ZhurnalObshcheiKhimii,1985,vol.55,#6,p.1327-1331]

[1]Gurevich,P.A.;Komina,T.V.;Klimentova,G.Yu.;Zykova,T.V.;Ruzal',G.I.[PharmaceuticalChemistryJournal,1984,vol.18,#7,p.489-490][Khimiko-FarmatsevticheskiiZhurnal,1984,vol.18,#7,p.833-835]

[2]Gurevich,P.A.;Komina,T.V.;Klimentova,G.Yu.;Zykova,T.V.;Ruzal',G.I.[PharmaceuticalChemistryJournal,1984,vol.18,#7,p.489-490][Khimiko-FarmatsevticheskiiZhurnal,1984,vol.18,#7,p.833-835]

[3]Gurevich,P.A.;Razumov,A.I.;Komina,T.V.;Klimentova,G.Yu.;Zykova,T.V.[JournalofgeneralchemistryoftheUSSR,1985,vol.55,#6,p.1187-1190][ZhurnalObshcheiKhimii,1985,vol.55,#6,p.1327-1331]

[1]Gurevich,P.A.;Komina,T.V.;Klimentova,G.Yu.;Zykova,T.V.;Ruzal',G.I.[PharmaceuticalChemistryJournal,1984,vol.18,#7,p.489-490][Khimiko-FarmatsevticheskiiZhurnal,1984,vol.18,#7,p.833-835]

[2]Gurevich,P.A.;Komina,T.V.;Klimentova,G.Yu.;Zykova,T.V.;Ruzal',G.I.[PharmaceuticalChemistryJournal,1984,vol.18,#7,p.489-490][Khimiko-FarmatsevticheskiiZhurnal,1984,vol.18,#7,p.833-835]

[3]Gurevich,P.A.;Razumov,A.I.;Komina,T.V.;Klimentova,G.Yu.;Zykova,T.V.[JournalofgeneralchemistryoftheUSSR,1985,vol.55,#6,p.1187-1190][ZhurnalObshcheiKhimii,1985,vol.55,#6,p.1327-1331]

Literature

Title: Substituted indole-1-acetic acids as potent and selective CRTh2 antagonists-discovery of AZD1981.

Journal: Bioorganic & medicinal chemistry letters 20111101

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