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Home Fluorides 367-29-3
367-29-3,MFCD00007764
Catalog No.:AA003MO9

367-29-3 | 5-Fluoro-2-methylaniline

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$7.00   $5.00
- +
10g
98%
in stock  
$9.00   $7.00
- +
25g
98%
in stock  
$17.00   $12.00
- +
100g
98%
in stock  
$23.00   $16.00
- +
500g
98%
in stock  
$103.00   $72.00
- +
  • 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:
AA003MO9
Chemical Name:
5-Fluoro-2-methylaniline
CAS Number:
367-29-3
Molecular Formula:
C7H8FN
Molecular Weight:
125.1435
MDL Number:
MFCD00007764
SMILES:
Fc1ccc(c(c1)N)C
NSC Number:
60730
Properties
Properties
 
BP:
203.3°C at 760 mmHg  
Form:
Liquid  
MP:
38-40 °C(lit.)  
Refractive Index:
1.538  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
94.9  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
XLogP3:
0.9  

Upstream Synthesis Route

[1]Patent:WO2015/104662,2015,A1,.Locationinpatent:Page/Pagecolumn37;38

[2]Patent:US2016/326151,2016,A1,.Locationinpatent:Paragraph0206

[3]BioorganicandMedicinalChemistry,2008,vol.16,#4,p.1966-1982

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

[5]BioorganicandMedicinalChemistry,2004,vol.12,#9,p.2115-2137

[1]BulletindesSocietesChimiquesBelges,1960,vol.69,p.312-322

[1]JournaloftheAmericanChemicalSociety,1985,vol.107,p.1556-1561

[1]Patent:US4243805,1981,A,

[1]CollectionofCzechoslovakChemicalCommunications,1979,vol.44,#7,p.2108-2123

Downstream Synthesis Route

[1]JournalofOrganicChemistry,1992,vol.57,p.5254-5255

[2]Patent:WO2015/104662,2015,A1.Locationinpatent:Page/Pagecolumn37

[3]Patent:US2016/326151,2016,A1.Locationinpatent:Paragraph0204

[4]JournaloftheAmericanChemicalSociety,1948,vol.70,p.439

[5]JournaloftheChemicalSociety,1953,p.3326

[6]CollectionofCzechoslovakChemicalCommunications,1975,vol.40,p.719-737

[7]CollectionofCzechoslovakChemicalCommunications,1979,vol.44,p.2108-2123

[8]JournaloftheChemicalSociety,1960,p.672-676

[9]JournaloftheAmericanChemicalSociety,1996,vol.118,p.4036-4048

[10]BioorganicandMedicinalChemistryLetters,2007,vol.17,p.3177-3180

[1]Patent:WO2005/30213,2005,A1.Locationinpatent:Page/Pagecolumn184-185

[2]Tetrahedron,1959,vol.6,p.315,316

[3]Patent:US2003/207924,2003,A1

[1]CurrentPatentAssignee:BRISTOL-MYERSSQUIBBCO-WO2016/4105,2016,A1Locationinpatent:Paragraph00146

[2]CurrentPatentAssignee:BIOSPLICETHERAPEUTICSINC-WO2017/24021,2017,A1Locationinpatent:Paragraph0622;0623

[3]CurrentPatentAssignee:BIOSPLICETHERAPEUTICSINC-WO2017/24013,2017,A1Locationinpatent:Paragraph0622;0623

[4]CurrentPatentAssignee:BIOSPLICETHERAPEUTICSINC-WO2017/24010,2017,A1Locationinpatent:Paragraph006;007

[5]CurrentPatentAssignee:BIOSPLICETHERAPEUTICSINC-WO2017/23986,2017,A1Locationinpatent:Paragraph0626;0627

[6]CurrentPatentAssignee:BIOSPLICETHERAPEUTICSINC-US2016/75701,2016,A1Locationinpatent:Paragraph0805;0806

[7]CurrentPatentAssignee:EISAICOLTD-US2016/347717,2016,A1Locationinpatent:Paragraph0619;0620

[8]Steck;Fletcher[JournaloftheAmericanChemicalSociety,1948,vol.70,p.439]

[9]CurrentPatentAssignee:EISAICOLTD-EP1510516,2005,A1Locationinpatent:Page/Pagecolumn101

[10]CurrentPatentAssignee:MERCK&COINC-WO2009/32123,2009,A2Locationinpatent:Page/Pagecolumn178-179

[11]CurrentPatentAssignee:MERCK&COINC-WO2009/32125,2009,A1Locationinpatent:Page/Pagecolumn118

[12]CurrentPatentAssignee:MERCK&COINC-WO2009/32124,2009,A1Locationinpatent:Page/Pagecolumn193

[13]CurrentPatentAssignee:AMGENINC-WO2006/44860,2006,A2Locationinpatent:Page/Pagecolumn37-38

[14]Venkatraman,Srikanth;Velazquez,Francisco;Gavalas,Stephen;Wu,Wanli;Chen,KevinX.;Nair,AnilkumarG.;Bennett,Frank;Huang,Yuhua;Pinto,Patrick;Jiang,Yueheng;Selyutin,Oleg;Vibulbhan,Bancha;Zeng,Qingbei;Lesburg,Charles;Duca,Jose;Heimark,Larry;Huang,Hsueh-Cheng;Agrawal,Sony;Jiang,Chuan-Kui;Ferrari,Eric;Li,Cheng;Kozlowski,Joseph;Rosenblum,Stuart;Shih,Neng-Yang;GeorgeNjoroge[BioorganicandMedicinalChemistry,2014,vol.22,#1,p.447-458]

[15]CurrentPatentAssignee:BIOSPLICETHERAPEUTICSINC-US2016/90380,2016,A1Locationinpatent:Paragraph0806

[1]BulletindesSocietesChimiquesBelges,1960,vol.69,p.312-322

[1]CollectionofCzechoslovakChemicalCommunications,1979,vol.44,p.2108-2123

Literature

Title: Isomer selective IR-UV depletion spectroscopy of 4-fluorotoluene-NH3: evidence for π-proton-acceptor and linear hydrogen-bonded complexes.

Journal: Physical chemistry chemical physics : PCCP 20110914

Title: The role of the methyl group in stabilising the weak N-H...pi hydrogen bond in the 4-fluorotoluene-ammonia complex.

Journal: Physical chemistry chemical physics : PCCP 20100107

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