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Home Thiazoles 939-69-5
939-69-5,MFCD00296905
Catalog No.:AA00GSLU

939-69-5 | 2-Cyano-6-hydroxybenzothiazole

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
97%
in stock  
$6.00   $4.00
- +
250mg
97%
in stock  
$7.00   $5.00
- +
1g
97%
in stock  
$17.00   $12.00
- +
5g
97%
in stock  
$71.00   $50.00
- +
10g
97%
in stock  
$126.00   $89.00
- +
25g
97%
in stock  
$315.00   $220.00
- +
  • 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:
AA00GSLU
Chemical Name:
2-Cyano-6-hydroxybenzothiazole
CAS Number:
939-69-5
Molecular Formula:
C8H4N2OS
Molecular Weight:
176.1952
MDL Number:
MFCD00296905
SMILES:
N#Cc1nc2c(s1)cc(cc2)O
Properties
Properties
 
BP:
374.7±34.0°C at 760 mmHg  
Form:
Solid  
MP:
195-200°C  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
224  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
XLogP3:
2.3  

Upstream Synthesis Route

[1]Patent:EP2754657,2014,A1,.Locationinpatent:Paragraph0088-0090

[2]Patent:US5616729,1997,A,

[3]OrganicandBiomolecularChemistry,2015,vol.13,#7,p.2117-2121

[4]Chemistry-AEuropeanJournal,2016,vol.22,#27,p.9330-9337

[5]Patent:JP6095208,2017,B2,.Locationinpatent:Paragraph0048-0050

[6]JournaloftheAmericanChemicalSociety,2013,vol.135,#5,p.1783-1795

[7]Patent:US2013/287699,2013,A1,.Locationinpatent:Paragraph0416

[8]Patent:US2013/315829,2013,A1,.Locationinpatent:Paragraph0188

[9]AngewandteChemie-InternationalEdition,2007,vol.46,#37,p.7031-7034

[10]Patent:CN105384704,2016,A,.Locationinpatent:Paragraph0046;0047

[11]BulletinoftheChemicalSocietyofJapan,1992,vol.65,#2,p.392-395

[12]ChemicalCommunications,2018,vol.54,#14,p.1774-1777

[13]BioconjugateChemistry,2012,vol.23,#9,p.1902-1908,7

[14]BioconjugateChemistry,2012,vol.23,#9,p.1902-1908

[15]EuropeanJournalofMedicinalChemistry,2015,vol.94,p.140-148

[16]ChemicalCommunications,2009,#27,p.4028-4030

[17]JournaloftheAmericanChemicalSociety,2010,vol.132,#25,p.8563-8565

[18]JournaloftheAmericanChemicalSociety,2012,vol.134,#18,p.7604-7607

[19]JournaloftheAmericanChemicalSociety,1963,vol.85,p.337-343

[1]Patent:US4826989,1989,A,

[1]Synlett,2009,#16,p.2682-2684

[1]OrganicandBiomolecularChemistry,2015,vol.13,#7,p.2117-2121

[1]OrganicandBiomolecularChemistry,2015,vol.13,#7,p.2117-2121

Downstream Synthesis Route

[1]Tetrahedron,1972,vol.28,p.4075-4082

[1]Tetrahedron,1972,vol.28,p.4065-4074

[1]JournalofOrganicChemistry,1965,vol.30,p.2344-2348

[1]JournaloftheAmericanChemicalSociety,1963,vol.85,p.337-343

[1]Tetrahedron,1972,vol.28,p.4065-4074

[2]JournaloftheAmericanChemicalSociety,2009,vol.131,p.11590-11605

Literature

Title: Applications of luciferin biosynthesis: Bioluminescence assays for l-cysteine and luciferase.

Journal: Analytical biochemistry 20100115

Title: Oxyluciferin, a luminescence product of firefly luciferase, is enzymatically regenerated into luciferin.

Journal: The Journal of biological chemistry 20010928

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