Home Iodos 13194-68-8
13194-68-8,MFCD00025299
Catalog No.:AA000ZVO

13194-68-8 | 4-Iodo-2-methylaniline

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5g
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98%
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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:
AA000ZVO
Chemical Name:
4-Iodo-2-methylaniline
CAS Number:
13194-68-8
Molecular Formula:
C7H8IN
Molecular Weight:
233.0496
MDL Number:
MFCD00025299
SMILES:
Ic1ccc(c(c1)C)N
NSC Number:
60731
Properties
Properties
 
BP:
278.4 °C at 760 mmHg  
Form:
Solid  
MP:
86-89 °C  
Stability:
Light Sensitive  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
94.9  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
XLogP3:
2  

Upstream Synthesis Route

[1]Patent:US2009/82359,2009,A1,.Locationinpatent:Page/Pagecolumn47

[2]BioorganicandMedicinalChemistryLetters,2007,vol.17,#11,p.3177-3180

[3]Patent:US2012/71535,2012,A1,.Locationinpatent:Page/Pagecolumn53-54

[4]Patent:WO2008/154241,2008,A1,

[1]AmericanChemicalJournal,1909,vol.42,p.500

[1]Synthesis(Germany),2014,vol.46,#8,p.1085-1090

[2]JournaloftheAmericanChemicalSociety,2015,vol.137,#26,p.8328-8331

[1]BulletinoftheChemicalSocietyofEthiopia,2015,vol.29,#1,p.157-162

[2]BulletinoftheChemicalSocietyofJapan,1988,vol.61,#2,p.600-602

[3]Molecules,2002,vol.7,#12,p.867-870

[4]Synthesis,2004,#3,p.441-445

[5]SyntheticCommunications,2012,vol.42,#16,p.2407-2414

[6]JournaloftheIranianChemicalSociety,2012,vol.9,#3,p.321-326

[7]Molecules,2005,vol.10,#10,p.1307-1317

[8]SyntheticCommunications,2013,vol.43,#21,p.2913-2925

[9]TetrahedronLetters,2011,vol.52,#52,p.7141-7145

[10]JournaloftheChineseChemicalSociety,1996,vol.43,#1,p.95-99

[11]Molecules,2004,vol.9,#7,p.617-621

[12]Patent:CN103497211,2016,B,.Locationinpatent:Paragraph0068;0069

[13]IndianJournalofChemistry,SectionA:Inorganic,Physical,Theoretical&Analytical,1987,vol.26,#4,p.333-335

[14]AmericanChemicalJournal,1909,vol.42,p.500

[15]ZhurnalObshcheiKhimii,1953,vol.23,p.663,666;engl.Ausg.S.689,691

[16]JournaloftheAmericanChemicalSociety,1925,vol.47,p.1711

[17]JournaloftheAmericanChemicalSociety,1941,vol.63,p.436

[18]CatalysisLetters,2010,vol.137,#3-4,p.190-201

[19]Synlett,2012,#2,p.208-214

[20]ChemicalCommunications,2014,vol.50,#17,p.2136-2138

[21]RSCAdvances,2015,vol.6,#1,p.403-408

[1]TetrahedronLetters,2007,vol.48,#35,p.6124-6128

[2]SyntheticCommunications,2008,vol.38,#22,p.3894-3902

[3]Synlett,2012,#2,p.208-214

Downstream Synthesis Route

[1]Patent:WO2015/86642,2015,A1.Locationinpatent:Page/Pagecolumn101

[2]JournalfurpraktischeChemie(Leipzig1954),1906,vol.<2>74,p.314

[1]Artmann[MonatsheftefurChemie,1905,vol.26,p.1103]

[1]BulletinoftheChemicalSocietyofEthiopia,2015,vol.29,p.157-162

[2]BulletinoftheChemicalSocietyofJapan,1988,vol.61,p.600-602

[3]Molecules,2002,vol.7,p.867-870

[4]Synthesis,2004,p.441-445

[5]SyntheticCommunications,2012,vol.42,p.2407-2414

[6]JournaloftheIranianChemicalSociety,2012,vol.9,p.321-326

[7]NewJournalofChemistry,2019,vol.43,p.6001-6009

[8]Molecules,2005,vol.10,p.1307-1317

[9]SyntheticCommunications,2013,vol.43,p.2913-2925

[10]TetrahedronLetters,2011,vol.52,p.7141-7145

[11]JournaloftheChineseChemicalSociety,1996,vol.43,p.95-99

[12]Molecules,2004,vol.9,p.617-621

[13]Patent:CN103497211,2016,B.Locationinpatent:Paragraph0068;0069

[14]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,1987,vol.26,p.333-335

[15]AmericanChemicalJournal,1909,vol.42,p.500

[16]ZhurnalObshcheiKhimii,1953,vol.23,p.663,666;engl.Ausg.S.689,691

[17]JournaloftheAmericanChemicalSociety,1925,vol.47,p.1711

[18]JournaloftheAmericanChemicalSociety,1941,vol.63,p.436

[19]CatalysisLetters,2010,vol.137,p.190-201

[20]Synlett,2012,p.208-214

[21]ChemicalCommunications,2014,vol.50,p.2136-2138

[22]RSCAdvances,2015,vol.6,p.403-408

[1]ChemicalandPharmaceuticalBulletin,1984,vol.32,p.305-312

[1]Ozawa;Takeuchi;Yamamoto;Hamada;Ito;Kuwahara;Takagaki[ChemicalandPharmaceuticalBulletin,1984,vol.32,#1,p.305-312]

Literature

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: 4-Iodo-2-methyl-aniline.

Journal: Acta crystallographica. Section E, Structure reports online 20080301

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