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Home Nitro Compounds 80866-88-2
80866-88-2,MFCD00007098
Catalog No.:AA0033O0

80866-88-2 | 3-Methoxy-4-nitrobenzyl alcohol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$16.00   $11.00
- +
1g
95%
in stock  
$24.00   $17.00
- +
5g
95%
in stock  
$88.00   $62.00
- +
10g
98%
in stock  
$94.00   $66.00
- +
25g
98%
in stock  
$233.00   $164.00
- +
  • 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:
AA0033O0
Chemical Name:
3-Methoxy-4-nitrobenzyl alcohol
CAS Number:
80866-88-2
Molecular Formula:
C8H9NO4
Molecular Weight:
183.1614
MDL Number:
MFCD00007098
SMILES:
COc1cc(CO)ccc1[N+](=O)[O-]
Properties
Properties
 
Form:
Solid  
MP:
95-97°C(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
180  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
0.8  

Upstream Synthesis Route

[1]Patent:EP2853565,2015,A1,.Locationinpatent:Paragraph0220

[2]BioorganicandMedicinalChemistry,2000,vol.8,#10,p.2417-2425

[3]AngewandteChemie-InternationalEdition,2018,vol.57,#24,p.7040-7045

[4]Angew.Chem.,2018,vol.130,#24,p.7158-7163,6

[5]Patent:EP3290419,2018,A1,.Locationinpatent:Paragraph0176;0177

[6]Patent:WO2012/151561,2012,A1,.Locationinpatent:Page/Pagecolumn71

[7]Patent:WO2013/169401,2013,A1,.Locationinpatent:Page/Pagecolumn84

[8]JournalofFluorineChemistry,2007,vol.128,#12,p.1461-1468

[1]BulletindelaSocieteChimiquedeFrance,1993,vol.130,#1,p.93-95

[2]Patent:WO2005/97752,2005,A1,.Locationinpatent:Page/Pagecolumn124-125

[3]Tetrahedron,2004,vol.60,#19,p.4295-4302

[4]Patent:US5994368,1999,A,

[5]Patent:US6008229,1999,A,

[6]Patent:US6083961,2000,A,

[7]Patent:US6344462,2002,B1,.Locationinpatent:Pagecolumn22

[8]Patent:WO2012/97683,2012,A1,.Locationinpatent:Page/Pagecolumn90

[9]Patent:US2014/171429,2014,A1,.Locationinpatent:Paragraph0375

Downstream Synthesis Route

[1]BulletindelaSocieteChimiquedeFrance,1993,vol.130,p.93-95

[2]Patent:WO2005/97752,2005,A1.Locationinpatent:Page/Pagecolumn124-125

[3]Tetrahedron,2004,vol.60,p.4295-4302

[4]Patent:US5994368,1999,A

[5]Patent:US6008229,1999,A

[6]Patent:US6083961,2000,A

[7]Patent:US6344462,2002,B1.Locationinpatent:Pagecolumn22

[8]Patent:WO2012/97683,2012,A1.Locationinpatent:Page/Pagecolumn90

[9]Patent:US2014/171429,2014,A1.Locationinpatent:Paragraph0375

[1]BioorganicandMedicinalChemistryLetters,2005,vol.15,p.4143-4150

[1]BioorganicandMedicinalChemistryLetters,2005,vol.15,p.4143-4150

[1]BioorganicandMedicinalChemistryLetters,2005,vol.15,p.4143-4150

80866-88-2   
(4-amino-3-methoxy-benzyl)-thiocarbamicacid<i>O</i>-(4-<i>tert</i>-butyl-benzyl)ester 

[1]BioorganicandMedicinalChemistryLetters,2005,vol.15,p.4143-4150

Literature
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SDS
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