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30095-98-8,MFCD00968465
Catalog No.:AA003RFL

30095-98-8 | Methyl 2-(2-nitrophenyl)acetate

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Purity
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Price(USD)
Quantity
  
1g
98%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$19.00   $14.00
- +
25g
98%
in stock  
$58.00   $41.00
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100g
98%
in stock  
$231.00   $162.00
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500g
98%
in stock  
$1,004.00   $703.00
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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:
AA003RFL
Chemical Name:
Methyl 2-(2-nitrophenyl)acetate
CAS Number:
30095-98-8
Molecular Formula:
C9H9NO4
Molecular Weight:
195.1721
MDL Number:
MFCD00968465
SMILES:
COC(=O)Cc1ccccc1[N+](=O)[O-]
Properties
Properties
 
BP:
283.4°C at 760 mmHg  
Form:
Solid  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
223  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
4  
Rotatable Bond Count:
3  
XLogP3:
1.9  

Upstream Synthesis Route

[1]Heterocycles,1996,vol.43,#12,p.2701-2712

[1]Patent:US2015/197511,2015,A1,

[1]Patent:EP1227084,2002,A1,

[2]Patent:CN106831436,2017,A,.Locationinpatent:Paragraph0016;0017;0019

[3]Patent:US5240938,1993,A,

[4]Patent:US2005/101587,2005,A9,

[5]AngewandteChemie-InternationalEdition,2012,vol.51,#2,p.548-551

[6]JournaloftheAmericanChemicalSociety,2015,vol.137,#3,p.1130-1135

[1]Tetrahedron,1997,vol.53,#48,p.16521-16532

[2]BioorganicandMedicinalChemistry,2003,vol.11,#18,p.3889-3899

[3]AngewandteChemie,InternationalEdition,2009,vol.48,#37,p.6892-6895

[4]AngewandteChemie,2009,vol.121,#37,p.7024-7027

[5]EuropeanJournalofOrganicChemistry,2017,vol.2017,#14,p.1889-1893

[6]ACSMedicinalChemistryLetters,2018,vol.9,#2,p.94-97

[7]AngewandteChemie-InternationalEdition,2018,vol.57,#31,p.9896-9900

[8]Angew.Chem.,2018,vol.130,p.10044-10048,5

[9]Patent:WO2014/106238,2014,A1,.Locationinpatent:Paragraph00213;00312;00339;00363;00396;00462;00497

[10]Patent:WO2014/106238,2014,A1,.Locationinpatent:Paragraph00268

[11]BioorganicandMedicinalChemistryLetters,2000,vol.10,#8,p.797-800

[12]AustralianJournalofChemistry,2013,vol.66,#8,p.864-873

[13]OrganicLetters,2009,vol.11,#6,p.1345-1348

[14]Heterocycles,1996,vol.43,#12,p.2701-2712

[15]OrganicandBiomolecularChemistry,2005,vol.3,#20,p.3805-3811

[16]Patent:WO2009/3970,2009,A1,.Locationinpatent:Page/Pagecolumn42-43

[17]BioorganicandMedicinalChemistryLetters,1997,vol.7,#10,p.1243-1248

[18]TetrahedronLetters,2003,vol.44,#2,p.331-334

[19]JournaloftheAmericanChemicalSociety,1983,vol.105,#1,p.74-79

[20]JournalofOrganicChemistry,1995,vol.60,#8,p.2326-2327

[21]BioorganicandMedicinalChemistryLetters,2003,vol.13,#17,p.2891-2893

[22]BioorganicandMedicinalChemistry,2005,vol.13,#14,p.4396-4401

[23]Patent:WO2006/91674,2006,A1,.Locationinpatent:Page/Pagecolumn70

[24]Patent:WO2009/80682,2009,A1,.Locationinpatent:Page/Pagecolumn51

[25]Patent:WO2003/82841,2003,A1,.Locationinpatent:Page/Pagecolumn90

[26]JournalofOrganicChemistry,2009,vol.74,#23,p.9222-9224

[27]Tetrahedron,2010,vol.66,#11,p.1980-1989

[28]OrganicLetters,2011,vol.13,#16,p.4240-4243

[29]Patent:WO2014/418,2014,A1,.Locationinpatent:Page/Pagecolumn59;60

[30]RSCAdvances,2014,vol.4,#84,p.44629-44633

[31]Patent:US2015/197511,2015,A1,.Locationinpatent:Paragraph0292;0293

[32]Chemistry-AEuropeanJournal,2016,vol.22,#19,p.6487-6490

[33]BioorganicandMedicinalChemistryLetters,2017,vol.27,#2,p.131-134

[1]Patent:CN108947861,2018,A,.Locationinpatent:Paragraph0023-0024

Downstream Synthesis Route

[1]Heterocycles,1983,vol.20,p.1797-1799

[1]Tetrahedron,1997,vol.53,p.16521-16532

[2]BioorganicandMedicinalChemistry,2003,vol.11,p.3889-3899

[3]AngewandteChemie-InternationalEdition,2009,vol.48,p.6892-6895    AngewandteChemie,2009,vol.121,p.7024-7027

[4]EuropeanJournalofOrganicChemistry,2017,vol.2017,p.1889-1893

[5]ACSMedicinalChemistryLetters,2018,vol.9,p.94-97

[6]AngewandteChemie-InternationalEdition,2018,vol.57,p.9896-9900    Angew.Chem.,2018,vol.130,p.10044-10048,5

[7]AngewandteChemie-InternationalEdition,2019,vol.58,p.7861-7865    Angew.Chem.,2019,vol.131,p.7943-7947,5

[8]Patent:WO2014/106238,2014,A1.Locationinpatent:Paragraph00213;00312;00339;00363;00396;00462;00497

[9]Patent:WO2014/106238,2014,A1.Locationinpatent:Paragraph00268

[10]OrganicLetters,2020,vol.22,p.322-325

[11]BioorganicandMedicinalChemistryLetters,2000,vol.10,p.797-800

[12]AustralianJournalofChemistry,2013,vol.66,p.864-873

[13]OrganicLetters,2009,vol.11,p.1345-1348

[14]Heterocycles,1996,vol.43,p.2701-2712

[15]OrganicandBiomolecularChemistry,2005,vol.3,p.3805-3811

[16]Patent:WO2009/3970,2009,A1.Locationinpatent:Page/Pagecolumn42-43

[17]BioorganicandMedicinalChemistryLetters,1997,vol.7,p.1243-1248

[18]TetrahedronLetters,2003,vol.44,p.331-334

[19]JournaloftheAmericanChemicalSociety,1983,vol.105,p.74-79

[20]JournalofOrganicChemistry,1995,vol.60,p.2326-2327

[21]BioorganicandMedicinalChemistryLetters,2003,vol.13,p.2891-2893

[22]BioorganicandMedicinalChemistry,2005,vol.13,p.4396-4401

[23]Patent:WO2006/91674,2006,A1.Locationinpatent:Page/Pagecolumn70

[24]Patent:WO2009/80682,2009,A1.Locationinpatent:Page/Pagecolumn51

[25]Patent:WO2003/82841,2003,A1.Locationinpatent:Page/Pagecolumn90

[26]JournalofOrganicChemistry,2009,vol.74,p.9222-9224

[27]Tetrahedron,2010,vol.66,p.1980-1989

[28]OrganicLetters,2011,vol.13,p.4240-4243

[29]Patent:WO2014/418,2014,A1.Locationinpatent:Page/Pagecolumn59;60

[30]RSCAdvances,2014,vol.4,p.44629-44633

[31]Patent:US2015/197511,2015,A1.Locationinpatent:Paragraph0292;0293

[32]Chemistry-AEuropeanJournal,2016,vol.22,p.6487-6490

[33]BioorganicandMedicinalChemistryLetters,2017,vol.27,p.131-134

[34]BioorganicandMedicinalChemistryLetters,2019,vol.29,p.1012-1018

[35]OrganicLetters,2019,vol.21,p.8049-8052

[1]HelveticaChimicaActa,2005,vol.88,p.891-904

30095-98-8    1493-27-2   
methyl2,2-bis(2-nitrophenyl)acetate 

[1]OrganicPreparationsandProceduresInternational,2005,vol.37,p.550-555

[1]AustralianJournalofChemistry,2004,vol.57,p.625-628

Literature

Title: Diastereoselective synthesis of substituted tetrahydroquinoline-4-carboxylic esters by a tandem reduction-reductive amination reaction.

Journal: The Journal of organic chemistry 20010420

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