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24434-84-2,MFCD08276872
Catalog No.:AA007N6X

24434-84-2 | Benzo[b]thiophene-3-carbonitrile

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$22.00   $15.00
- +
1g
98%
in stock  
$26.00   $18.00
- +
5g
98%
in stock  
$119.00   $83.00
- +
10g
98%
in stock  
$236.00   $165.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA007N6X
Chemical Name:
Benzo[b]thiophene-3-carbonitrile
CAS Number:
24434-84-2
Molecular Formula:
C9H5NS
Molecular Weight:
159.2077
MDL Number:
MFCD08276872
SMILES:
N#Cc1csc2c1cccc2
Properties
Computed Properties
 
Complexity:
193  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
XLogP3:
2.8  

Upstream Synthesis Route

[1]BulletindesSocietesChimiquesBelges,1983,vol.92,#1,p.53-60

[1]Molecules,2016,vol.21,#1,

[2]OrganicandBiomolecularChemistry,2016,vol.14,#5,p.1840-1840

[3]TetrahedronLetters,2013,vol.54,#17,p.2177-2179

[4]OrganicandBiomolecularChemistry,2015,vol.13,#30,p.8322-8329

[1]JournaloftheAmericanChemicalSociety,2003,vol.125,#10,p.2890-2891

[2]Patent:WO2004/13094,2004,A2,.Locationinpatent:Page47

[1]OrganicLetters,2015,vol.17,#2,p.202-205

[2]JournalofOrganicChemistry,2011,vol.76,#2,p.665-668

[1]OrganicLetters,2016,vol.18,#4,p.860-863

Downstream Synthesis Route

[1]JournalofMedicinalChemistry,1992,vol.35,p.1019-1031

917-54-4    74313-25-0    24434-84-2    30447-36-0    73798-99-9   
1-(2-Methylsulfanyl-benzobthiophen-3-yl)-ethanone 

[1]BulletindesSocietesChimiquesBelges,1983,vol.92,p.53-60

[1]JournaloftheChemicalSociety.PerkintransactionsI,1992,p.333-336

[1]Synlett,2006,p.2016-2020

[2]BioorganicandMedicinalChemistry,2007,vol.15,p.4482-4497

[1]Synlett,2006,p.2016-2020

Literature

Title: Synthesis and evaluation of benzo[b]thiophene derivatives as inhibitors of alkaline phosphatases.

Journal: Bioorganic & medicinal chemistry 20091015

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