Home Nitro Compounds 58032-84-1
58032-84-1,MFCD01859935
Catalog No.:AA003JQY

58032-84-1 | 3-Nitrophenylmethanesulfonyl chloride

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Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$60.00   $42.00
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5g
98%
in stock  
$163.00   $114.00
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10g
98%
in stock  
$309.00   $217.00
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25g
98%
in stock  
$726.00   $509.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003JQY
Chemical Name:
3-Nitrophenylmethanesulfonyl chloride
CAS Number:
58032-84-1
Molecular Formula:
C7H6ClNO4S
Molecular Weight:
235.6448
MDL Number:
MFCD01859935
SMILES:
[O-][N+](=O)c1cccc(c1)CS(=O)(=O)Cl
Properties
Properties
 
BP:
393.2°C at 760 mmHg  
Form:
Solid  
MP:
95-100℃  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
305  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
4  
Rotatable Bond Count:
2  
XLogP3:
2.1  

Downstream Synthesis Route

[1]CurrentPatentAssignee:CATALYSTTHERAPEUTICS-WO2015/172203,2015,A1Locationinpatent:Page/Pagecolumn91

[2]CurrentPatentAssignee:ASTRAZENECAPLC-US2010/184789,2010,A1Locationinpatent:Page/Pagecolumn13

[3]CurrentPatentAssignee:ASTRAZENECAPLC-WO2008/129070,2008,A1Locationinpatent:Page/Pagecolumn37

[4]CurrentPatentAssignee:ASTRAZENECAPLC-WO2008/129080,2008,A1Locationinpatent:Page/Pagecolumn108-115;129-130;135-136;157;174

[5]CurrentPatentAssignee:MERCKKGAA-WO2009/124962,2009,A2Locationinpatent:Page/Pagecolumn112

[6]Purgotti;Monti[GazzettaChimicaItaliana,1900,vol.30II,p.254]

[7]CurrentPatentAssignee:G1THERAPEUTICSINC-WO2019/136244,2019,A1Locationinpatent:Page/Pagecolumn153

[1]Ziegler;Sprague[JournalofOrganicChemistry,1951,vol.16,p.621,622,624]

[2]Morgan,M.Thomas;Bagchi,Pritha;Fahrni,ChristophJ.[JournaloftheAmericanChemicalSociety,2011,vol.133,#40,p.15906-15909]

[1]Rossi,S.;Maiorana,S.[TetrahedronLetters,1966,p.263-267]

[1]Tuchapskii,I.M.;Vizgert,R.V.[JournalofOrganicChemistryUSSR(EnglishTranslation),1975,vol.11,p.1901-1905][ZhurnalOrganicheskoiKhimii,1975,vol.11,p.1890-1894]

[1]Tuchapskii,I.M.;Vizgert,R.V.[JournalofOrganicChemistryUSSR(EnglishTranslation),1975,vol.11,p.1901-1905][ZhurnalOrganicheskoiKhimii,1975,vol.11,p.1890-1894]

[2]CurrentPatentAssignee:HUTCHISONCHINAMEDITECHLTD.-CN114085214,2022,ALocationinpatent:Paragraph0085-0089

Literature

Title: Synthesis of sulfonamide-based kinase inhibitors from sulfonates by exploiting the abrogated SN2 reactivity of 2,2,2-trifluoroethoxysulfonates.

Journal: Organic & biomolecular chemistry 20100521

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SDS
Tags:58032-84-1 Molecular Formula|58032-84-1 MDL|58032-84-1 SMILES|58032-84-1 3-Nitrophenylmethanesulfonyl chloride