Catalog No.:AA003MLS

17200-29-2 | 5-Chlorobenzoxazole

Name: Name:5-Chlorobenzoxazole
Brand: AABLOCKS
SKU: AA003MLS
Availability: InStock
Rating: 90 (10 reviews)

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250mg

98%

in stock

$8.00 $6.00

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98%

in stock

$11.00 $8.00

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10g

98%

in stock

$21.00 $15.00

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25g

98%

in stock

$25.00 $18.00

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100g

98%

in stock

$97.00 $68.00

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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003MLS

Chemical Name:

5-Chlorobenzoxazole

CAS Number:

17200-29-2

Molecular Formula:

C7H4ClNO

Molecular Weight:

153.5658

MDL Number:

MFCD00216939

SMILES:

Clc1ccc2c(c1)nco2

NSC Number:

24984

Properties

BP:

226.3°C at 760 mmHg

Form:

Solid

MP:

42-46 °C

Refractive Index:

1.5618 (estimate)

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

131

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

XLogP3:

2.2

Upstream Synthesis Route

17200-29-2

3621-81-6

[1]TetrahedronLetters,2012,vol.53,#7,p.730-732

122-51-0

95-85-2

17200-29-2

[1]ComptesRendusChimie,2013,vol.16,#11,p.1029-1034

[2]CombinatorialChemistryandHighThroughputScreening,2013,vol.16,#8,p.618-627

[3]MonatsheftefurChemie,2007,vol.138,#7,p.663-667

[4]AngewandteChemie-InternationalEdition,2012,vol.51,#19,p.4666-4670

[5]MonatsheftefurChemie,2011,vol.142,#1,p.87-91

[6]ChemicalCommunications,2014,vol.50,#73,p.10661-10664

[7]OrganicPreparationsandProceduresInternational,2013,vol.45,#1,p.57-65

[8]OrganicLetters,2011,vol.13,#3,p.522-525

[9]TetrahedronLetters,2012,vol.53,#34,p.4588-4590

[10]AngewandteChemie-InternationalEdition,2011,vol.50,#48,p.11511-11515

[11]ChemicalCommunications,2015,vol.51,#81,p.15059-15062

[12]TetrahedronLetters,2015,vol.56,#3,p.511-513

[13]JournalofOrganicChemistry,2011,vol.76,#13,p.5444-5449

[14]OrganicandBiomolecularChemistry,2012,vol.10,#18,p.3715-3720

[15]OrganicLetters,2010,vol.12,#15,p.3567-3569

[16]JournalofMolecularCatalysisA:Chemical,2010,vol.328,#1-2,p.119-123

[17]ChemicalCommunications,2011,vol.47,#41,p.11522-11524

[18]ChemicalCommunications,2012,vol.48,#42,p.5181-5183

[19]AngewandteChemie-InternationalEdition,2012,vol.51,#28,p.6993-6997

[20]AngewandteChemie-InternationalEdition,2013,vol.52,#16,p.4457-4461

[21]Angew.Chem.,2013,vol.125,#16,p.4553-4557,5

[22]JournalofOrganicChemistry,2016,vol.81,#23,p.11743-11750

[23]TetrahedronLetters,2019,vol.60,#1,p.68-71

95-85-2

149-73-5

17200-29-2

[1]Patent:US2016/168138,2016,A1,.Locationinpatent:Paragraph0118-0119

[2]CombinatorialChemistryandHighThroughputScreening,2013,vol.16,#8,p.618-627

[3]JournalofChemicalSciences,2014,vol.126,#3,p.579-585

[4]MonatsheftefurChemie,2011,vol.142,#1,p.87-91

[5]JournalofMolecularCatalysisA:Chemical,2010,vol.328,#1-2,p.119-123

[6]OrganicLetters,2012,vol.14,#13,p.3458-3461

[7]Patent:WO2012/148553,2012,A1,.Locationinpatent:Page/Pagecolumn39-40

[8]Patent:US9441254,2016,B2,.Locationinpatent:Paragraph10;11

61-80-3

17200-29-2

[1]ChemicalandPharmaceuticalBulletin,1997,vol.45,#9,p.1547-1549

123-39-7

95-85-2

17200-29-2

[1]JournalofPharmaceuticalSciences,1964,vol.53,p.538-544

Downstream Synthesis Route

61-80-3

17200-29-2

[1]ChemicalandPharmaceuticalBulletin,1997,vol.45,p.1547-1549

17200-29-2

13589-72-5

[1]JournaloftheAmericanChemicalSociety,2004,vol.126,p.8197-8205

73183-34-3

17200-29-2

936902-12-4

[1]Patent:US2007/112005,2007,A1.Locationinpatent:Page/Pagecolumn83

[2]Patent:US2007/280928,2007,A1.Locationinpatent:Page/Pagecolumn81

59919-11-8

17200-29-2

1158999-45-1

611-70-1

[1]Arisawa,Mieko;Toriyama,Fumihiko;Yamaguchi,Masahiko[TetrahedronLetters,2011,vol.52,#18,p.2344-2347]

17200-29-2

61-80-3

[1]Synlett,2012,p.97-100

Literature

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