Catalog No.:AA003332

63604-94-4 | 2-Bromo-5-methoxyphenol

Name: Name:2-Bromo-5-methoxyphenol
Brand: AABLOCKS
SKU: AA003332
Availability: InStock
Rating: 90 (10 reviews)

Pack Size

Purity

Availability

Price(USD)

Quantity

250mg

98%

in stock

$6.00 $4.00

- +

98%

in stock

$8.00 $6.00

- +

98%

in stock

$31.00 $22.00

- +

10g

98%

in stock

$52.00 $36.00

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25g

98%

in stock

$115.00 $81.00

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100g

98%

in stock

$366.00 $256.00

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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:

AA003332

Chemical Name:

2-Bromo-5-methoxyphenol

CAS Number:

63604-94-4

Molecular Formula:

C7H7BrO2

Molecular Weight:

203.0333

MDL Number:

MFCD03428523

SMILES:

COc1ccc(c(c1)O)Br

Properties

BP:

253.3°C at 760 mmHg

Form:

Solid

MP:

152 °C

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

108

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

2.5

Upstream Synthesis Route

63604-94-4

23681-89-2

[1]Patent:WO2017/218960,2017,A1,

6626-15-9

77-78-1

17715-69-4

63604-94-4

[1]JournaloftheAmericanChemicalSociety,1926,vol.48,p.3127

150-19-6

63604-94-4

[1]SyntheticCommunications,2007,vol.37,#2,p.323-328

[2]EuropeanJournalofOrganicChemistry,2015,vol.2015,#11,p.2470-2481

[3]JournaloftheSerbianChemicalSociety,2011,vol.76,#5,p.685-692

[4]BioorganicandMedicinalChemistry,2017,vol.25,#22,p.6175-6177

[5]JournalofMedicinalChemistry,2002,vol.45,#18,p.3972-3983

[6]AngewandteChemie-InternationalEdition,2012,vol.51,#12,p.2925-2929

[7]JournalofOrganicChemistry,2016,vol.81,#20,p.9765-9774

[8]Patent:WO2016/149393,2016,A1,.Locationinpatent:Paragraph0326

[9]Patent:WO2012/125926,2012,A2,.Locationinpatent:Page/Pagecolumn80

[10]Patent:WO2012/122716,2012,A1,.Locationinpatent:Page/Pagecolumn99

[11]ChemicalCommunications,2018,vol.54,#39,p.4935-4938

[12]AngewandteChemie-InternationalEdition,2007,vol.46,#9,p.1448-1450

[13]DaltonTransactions,2013,vol.42,#12,p.4218-4222

[14]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1983,#12,p.2927-2932

[15]JournaloftheChemicalSociety,ChemicalCommunications,1980,#22,p.1103-1104

[16]OrganicLetters,2003,vol.5,#20,p.3679-3682

[17]Patent:US6365602,2002,B1,

[18]Patent:WO2010/145203,2010,A1,.Locationinpatent:Page/Pagecolumn43-44

[19]Patent:WO2017/218960,2017,A1,.Locationinpatent:Paragraph00389

150-19-6

63604-94-4

102127-34-4

[1]Synlett,1997,vol.1997,#11,p.1241-1242

[2]Synlett,1997,vol.1997,#11,p.1241-1242

[3]Patent:US7045545,2006,B1,.Locationinpatent:Page/Pagecolumn19

[4]Patent:EP1204659,2003,B1,.Locationinpatent:Page/Pagecolumn14

[5]BeilsteinJournalofOrganicChemistry,2014,vol.10,p.622-627

150-19-6

63604-94-4

[1]Patent:US5849732,1998,A,

Downstream Synthesis Route

150-19-6

63604-94-4

102127-34-4

[1]Synlett,1997,vol.1997,p.1241-1242

[2]Patent:CN110317129,2019,A.Locationinpatent:Paragraph0092-0095

[3]Synlett,1997,vol.1997,p.1241-1242

[4]Patent:US7045545,2006,B1.Locationinpatent:Page/Pagecolumn19

[5]Patent:EP1204659,2003,B1.Locationinpatent:Page/Pagecolumn14

[6]BeilsteinJournalofOrganicChemistry,2014,vol.10,p.622-627

150-19-6

63604-94-4

39835-11-5

102127-34-4

4584-46-7

548785-39-3

[1]Patent:US6617346,2003,B1

63604-94-4

132559-91-2

1259312-83-8

[1]DaltonTransactions,2010,vol.39,p.10391-10400

63604-94-4

132559-91-2

1259312-70-3

[1]DaltonTransactions,2010,vol.39,p.10391-10400

Literature

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SDS