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Home Aldehydes 20035-41-0
20035-41-0,MFCD00046152
Catalog No.:AA002CMN

20035-41-0 | 6-Bromo-2-hydroxy-3-methoxybenzaldehyde

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10mg
97%
in stock  
$6.00   $4.00
- +
50mg
97%
in stock  
$7.00   $5.00
- +
250mg
97%
in stock  
$12.00   $8.00
- +
1g
97%
in stock  
$22.00   $15.00
- +
5g
97%
in stock  
$71.00   $50.00
- +
25g
>99.0%(GC)(T)
in stock  
$322.00   $225.00
- +
100g
96%
in stock  
$926.00   $648.00
- +
  • 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:
AA002CMN
Chemical Name:
6-Bromo-2-hydroxy-3-methoxybenzaldehyde
CAS Number:
20035-41-0
Molecular Formula:
C8H7BrO3
Molecular Weight:
231.0434
MDL Number:
MFCD00046152
SMILES:
COc1ccc(c(c1O)C=O)Br
NSC Number:
95682
Properties
Properties
 
BP:
282.1°C at 760 mmHg  
Form:
Solid  
MP:
102-105 °C(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
162  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
2.1  

Upstream Synthesis Route

[1]Patent:CN108358761,2018,A,.Locationinpatent:Paragraph0042;0043;0078;0079;0096;0097;0105;0106

[2]JournalofMedicinalChemistry,2000,vol.43,#14,p.2731-2737

[3]Patent:US2003/220304,2003,A1,

[4]Patent:US2006/293394,2006,A1,.Locationinpatent:Figure12

[5]TetrahedronLetters,2003,vol.44,#27,p.5129-5132

[6]ACH-ModelsinChemistry,1994,vol.131,#2,p.217-228

[7]Patent:CN106905154,2017,A,.Locationinpatent:Paragraph0080;0085;0086

[8]Patent:CN107266304,2017,A,.Locationinpatent:Paragraph0014;0031;0032;0035

[1]Patent:CN108484593,2018,A,.Locationinpatent:Paragraph0044;0045;0062

[2]JournalofOrganicChemistry,1987,vol.52,#20,p.4485-4489

[3]AustralianJournalofChemistry,1976,vol.29,p.2003-2021

[4]AustralianJournalofChemistry,1994,vol.47,#5,p.951-956

[5]TetrahedronLetters,2003,vol.44,#27,p.5129-5132

[6]JournalofMedicinalChemistry,2000,vol.43,#14,p.2731-2737

[7]ACH-ModelsinChemistry,1994,vol.131,#2,p.217-228

[8]Patent:CN106905154,2017,A,

[9]Patent:CN107266304,2017,A,

[10]Patent:CN108358761,2018,A,

[1]TetrahedronLetters,2003,vol.44,#27,p.5129-5132

[2]JournalofOrganicChemistry,1987,vol.52,#20,p.4485-4489

[3]BioorganicandMedicinalChemistryLetters,2010,vol.20,#3,p.1090-1093

[4]BioorganicandMedicinalChemistryLetters,2010,vol.20,#12,p.3768-3771

[5]Patent:CN106905154,2017,A,

[6]Patent:CN107266304,2017,A,

[7]Patent:CN108358761,2018,A,

[8]Patent:CN108358761,2018,A,

[9]Patent:CN108484593,2018,A,

[1]AngewandteChemie-InternationalEdition,2018,vol.57,#2,p.465-469

[2]Angew.Chem.,2018,vol.130,#2,p.474-478,5

[3]AngewandteChemie-InternationalEdition,2018,vol.57,#2,p.465-469

[4]Angew.Chem.,2018,vol.130,#2,p.474-478,5

[5]OrganicLetters,2018,vol.20,#19,p.6284-6288

[1]ZeitschriftfuerNaturforschung,TeilB:AnorganischeChemie,OrganischeChemie,1986,vol.41,#10,p.1273-1280

Downstream Synthesis Route

[1]EuropeanJournalofMedicinalChemistry,1977,vol.12,p.385-386

[2]Patent:WO2005/85222,2005,A1.Locationinpatent:Page/Pagecolumn60-61

[1]OrganicandBiomolecularChemistry,2014,vol.12,p.7338-7344

[2]Synlett,2015,vol.26,p.1175-1178

[3]Tetrahedron,2015,vol.71,p.8172-8177

[4]Patent:CN106905154,2017,A.Locationinpatent:Paragraph0080;0087;0088

[5]Patent:CN107266304,2017,A.Locationinpatent:Paragraph0014;0031;0032;0036

[6]Patent:US2016/145304,2016,A1.Locationinpatent:Paragraph0393;0394;0395;0396

[7]Tetrahedron,2013,vol.69,p.4670-4678

[8]Patent:WO2016/1834,2016,A1.Locationinpatent:Page/Pagecolumn46;47

[9]AngewandteChemie-InternationalEdition,2020,vol.59,p.775-779    Angew.Chem.,2020,vol.132,p.785-789,5

[10]ZeitschriftfurNaturforschung,TeilB:AnorganischeChemie,OrganischeChemie,1986,vol.41,p.1273-1280

[11]Molecules,2019,vol.24

[1]Patent:CN108484593,2018,A.Locationinpatent:Paragraph0044;0045;0062

[2]JournalofOrganicChemistry,1987,vol.52,p.4485-4489

[3]AustralianJournalofChemistry,1976,vol.29,p.2003-2021

[4]AustralianJournalofChemistry,1994,vol.47,p.951-956

[5]TetrahedronLetters,2003,vol.44,p.5129-5132

[6]JournalofMedicinalChemistry,2000,vol.43,p.2731-2737

[7]ACH-ModelsinChemistry,1994,vol.131,p.217-228

[8]Patent:CN106905154,2017,A

[9]Patent:CN107266304,2017,A

[10]Patent:CN108358761,2018,A

[11]Tetrahedron,2018,vol.74,p.5996-6002

[12]Molecules,2019,vol.24

[13]Patent:US2020/108083,2020,A1

[1]JournalofOrganicChemistry,1998,vol.63,p.4235-4239

[2]TetrahedronLetters,2003,vol.44,p.5129-5132

[3]JournalofOrganicChemistry,1988,vol.53,p.1708-1713

[1]AustralianJournalofChemistry,1994,vol.47,p.951-956

[2]JournalofMedicinalChemistry,2008,vol.51,p.6699-6710

Literature

Title: Potent and selective inhibitors of the inositol-requiring enzyme 1 endoribonuclease.

Journal: The Journal of biological chemistry 20110408

Title: John Bruce Patterson, et al. Ire-1a inhibitors. WO 2008154484 A1

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SDS
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