Catalog No.:AA002SHU

26278-79-5 | 2-Amino-benzothiazol-6-ol

Name: Name:2-Amino-benzothiazol-6-ol
Brand: AABLOCKS
SKU: AA002SHU
Availability: InStock
Rating: 90 (10 reviews)

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250mg

97%

in stock

$6.00 $4.00

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97%

in stock

$7.00 $5.00

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97%

in stock

$18.00 $13.00

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10g

95%

in stock

$31.00 $22.00

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25g

97%

in stock

$75.00 $53.00

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100g

97%

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$268.00 $188.00

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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:

AA002SHU

Chemical Name:

2-Amino-benzothiazol-6-ol

CAS Number:

26278-79-5

Molecular Formula:

C7H6N2OS

Molecular Weight:

166.2003

MDL Number:

MFCD00511763

SMILES:

Oc1ccc2c(c1)sc(n2)N

Properties

BP:

394.6°C at 760 mmHg

Form:

Solid

MP:

243-250℃

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

155

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

XLogP3:

1.9

Upstream Synthesis Route

1520-27-0

26278-79-5

[1]BioorganicandMedicinalChemistryLetters,2017,vol.27,#15,p.3460-3463

[2]MedicinalChemistryResearch,2012,vol.21,#7,p.1136-1148

[3]JournalofMedicinalChemistry,2016,vol.59,#21,p.9814-9824

1753-90-8

26278-79-5

[1]Patent:WO2017/218960,2017,A1,.Locationinpatent:Paragraph00456

1747-60-0

26278-79-5

[1]Patent:WO2010/54058,2010,A1,.Locationinpatent:Page/Pagecolumn73-75

[2]Patent:WO2011/56939,2011,A1,.Locationinpatent:Page/Pagecolumn69-71

[3]EuropeanJournalofMedicinalChemistry,2016,vol.115,p.201-216

[4]Chemistry-AEuropeanJournal,2015,vol.21,#7,p.2893-2904

[5]ACSMedicinalChemistryLetters,2012,vol.3,#1,p.58-62

[6]JournalofPharmaceuticalSciences,1994,vol.83,#10,p.1425-1432

[7]UkrainskiiKhimicheskiiZhurnal(RussianEdition),1955,vol.21,p.344

[8]Chem.Abstr.,1955,p.14738

[9]JournalofHeterocyclicChemistry,1973,vol.10,#5,p.769-772

[10]JournaloftheChemicalSociety,PerkinTransactions2:PhysicalOrganicChemistry(1972-1999),1987,p.1781-1784

[11]Patent:WO2009/38757,2009,A2,.Locationinpatent:Page/Pagecolumn87

[12]Patent:EP2181987,2010,A1,.Locationinpatent:Page/Pagecolumn66

[13]Patent:WO2013/43001,2013,A1,.Locationinpatent:Paragraph1082;1083

[14]ArchivderPharmazie,2014,vol.347,#4,p.268-275

[15]Patent:US2015/11528,2015,A1,.Locationinpatent:Paragraph0608

[16]Molecules,2016,vol.21,#3,

[17]Molecules,2016,vol.21,#2,

[18]Patent:US2017/12072,2017,A1,.Locationinpatent:Paragraph0477;0478;0479

[19]BioorganicandMedicinalChemistry,2017,vol.25,#14,p.3614-3622

94-45-1

26278-79-5

[1]Patent:US2007/93488,2007,A1,.Locationinpatent:Page/Pagecolumn7

[2]Patent:US2008/194555,2008,A1,.Locationinpatent:Page/Pagecolumn20

1747-60-0

26278-79-5

[1]Patent:US2004/142953,2004,A1,

[2]Patent:US2005/288282,2005,A1,

[3]Patent:US6897220,2005,B2,

Downstream Synthesis Route

1747-60-0

26278-79-5

[1]Patent:WO2010/54058,2010,A1.Locationinpatent:Page/Pagecolumn73-75

[2]Patent:WO2011/56939,2011,A1.Locationinpatent:Page/Pagecolumn69-71

[3]EuropeanJournalofMedicinalChemistry,2016,vol.115,p.201-216

[4]ChemicalCommunications,2019,vol.55,p.790-793

[5]Chemistry-AEuropeanJournal,2015,vol.21,p.2893-2904

[6]ACSMedicinalChemistryLetters,2012,vol.3,p.58-62

[7]JournalofPharmaceuticalSciences,1994,vol.83,p.1425-1432

[8]UkrainskijKhimicheskijZhurnal,1955,vol.21,p.344 Chem.Abstr.,1955,p.14738

[9]JournalofHeterocyclicChemistry,1973,vol.10,p.769-772

[10]JournaloftheChemicalSociety.PerkintransactionsII,1987,p.1781-1784

[11]Patent:WO2009/38757,2009,A2.Locationinpatent:Page/Pagecolumn87

[12]Patent:EP2181987,2010,A1.Locationinpatent:Page/Pagecolumn66

[13]Patent:WO2013/43001,2013,A1.Locationinpatent:Paragraph1082;1083

[14]ArchivderPharmazie,2014,vol.347,p.268-275

[15]Molecules,2016,vol.21

[16]Patent:US2017/12072,2017,A1.Locationinpatent:Paragraph0477;0478;0479

[17]BioorganicandMedicinalChemistry,2017,vol.25,p.3614-3622

[18]JournalofEnzymeInhibitionandMedicinalChemistry,2019,vol.34,p.829-837

[19]Patent:US2015/11528,2015,A1.Locationinpatent:Paragraph0608

[20]InternationalJournalofMolecularSciences,2020,vol.21

26278-79-5

27475-19-0

99582-94-2

[1]JournalofMedicinalChemistry,1986,vol.29,p.386-394

26278-79-5

949557-20-4

6-(3-methyl-1H-pyrazolo3,4-bpyridin-4-yloxy)benzodthiazol-2-amine

[1]Patent:US2007/238726,2007,A1.Locationinpatent:Page/Pagecolumn85

26278-79-5

35654-56-9

6-(6,7-dimethoxyquinolin-4-yloxy)benzodthiazol-2-amine

[1]BioorganicandMedicinalChemistryLetters,2009,vol.19,p.1442-1445

[2]Patent:WO2005/73224,2005,A2.Locationinpatent:Page/Pagecolumn52

26278-79-5

24424-99-5

865861-31-0

[1]Patent:US2007/93488,2007,A1.Locationinpatent:Page/Pagecolumn10

Literature

Title: Studying the photoprotective activity of a new class of heteroaromatic antioxidants.

Journal: Bulletin of experimental biology and medicine 20090201

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

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SDS