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1073-72-9,MFCD00002351
Catalog No.:AA0033R1

1073-72-9 | 4-(Methylthio)phenol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$8.00   $6.00
- +
5g
98%
in stock  
$11.00   $8.00
- +
10g
98%
in stock  
$13.00   $9.00
- +
25g
98%
in stock  
$31.00   $22.00
- +
100g
98%
in stock  
$48.00   $34.00
- +
  • 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:
AA0033R1
Chemical Name:
4-(Methylthio)phenol
CAS Number:
1073-72-9
Molecular Formula:
C7H8OS
Molecular Weight:
140.2028
MDL Number:
MFCD00002351
SMILES:
CSc1ccc(cc1)O
NSC Number:
75840
Properties
Properties
 
BP:
269.7°C at 760 mmHg  
Form:
Solid  
MP:
84-86(lit.)  
Refractive Index:
1.5530 (estimate)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
77  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2.1  

Upstream Synthesis Route

[1]BioorganicandMedicinalChemistryLetters,2011,vol.21,#3,p.1015-1018

[1]Patent:WO2014/79497,2014,A1,.Locationinpatent:Page/Pagecolumn6;7

[1]Patent:WO2015/35223,2015,A1,.Locationinpatent:Paragraph0821

[2]Patent:WO2016/57242,2016,A1,.Locationinpatent:Paragraph0197

[3]JournaloftheAmericanChemicalSociety,2009,vol.131,#40,p.14190-14191

[4]AngewandteChemie-InternationalEdition,2011,vol.50,#21,p.4983-4987

[5]EuropeanJournalofOrganicChemistry,2014,vol.2014,#27,p.6077-6083

[6]Patent:WO2016/145236,2016,A1,.Locationinpatent:Paragraph0243-0244

[1]Patent:US2002/103141,2002,A1,

[2]Patent:US6034256,2000,A,

[1]Patent:US6077850,2000,A,

Downstream Synthesis Route

[1]Patent:DE2509037,1976,    Chem.Abstr.,1976,vol.85

[2]Patent:DE2722537,1978,    Chem.Abstr.,1979,vol.90

500-98-1    1073-72-9   
Phenylacetylamino-aceticacid4-methylsulfanyl-phenylester 

[1]Synthesis,1994,vol.1,p.480-482

[1]BioorganicandMedicinalChemistry,1997,vol.5,p.779-786

[1]Do,QuangTho;Elothmani,Driss;LeGuillanton,Georges[TetrahedronLetters,1998,vol.39,#26,p.4657-4658]

[2]Glass,RichardS.;Jouikov,ViatcheslavV.[TetrahedronLetters,1999,vol.40,#35,p.6357-6358]

1073-72-9    478068-00-7   
N-(2-(trifluoromethyl)pyridin-4-yl)anthranilicacid4-methylthiophenylester 

[1]Congiu,Cenzo;Cocco,MariaTeresa;Lilliu,Valentina;Onnis,Valentina[JournalofMedicinalChemistry,2005,vol.48,#26,p.8245-8252]

[2]Cocco,MariaT.;Congiu,Cenzo;Lilliu,Valentina;Onnis,Valentina[BioorganicandMedicinalChemistryLetters,2004,vol.14,#23,p.5787-5791]

Literature

Title: Transition-metal-free highly efficient aerobic oxidation of sulfides to sulfoxides under mild conditions.

Journal: Molecules (Basel, Switzerland) 20091228

Title: Dimerization of ionized 4-(methyl mercapto)-phenol during ESI, APCI and APPI mass spectrometry.

Journal: Journal of mass spectrometry : JMS 20090901

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