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63071-10-3,MFCD07437885
Catalog No.:AA003BSO

63071-10-3 | 4-Chloro-2-hydroxymethylpyridine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$11.00   $8.00
- +
5g
98%
in stock  
$17.00   $12.00
- +
10g
98%
in stock  
$21.00   $15.00
- +
25g
98%
in stock  
$50.00   $35.00
- +
100g
98%
in stock  
$195.00   $137.00
- +
  • 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:
AA003BSO
Chemical Name:
4-Chloro-2-hydroxymethylpyridine
CAS Number:
63071-10-3
Molecular Formula:
C6H6ClNO
Molecular Weight:
143.5709
MDL Number:
MFCD07437885
SMILES:
OCc1cc(Cl)ccn1
Properties
Properties
 
BP:
238.6°C at 760 mmHg  
Form:
Liquid  
MP:
68 - 69 °C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
89.1  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
0.6  

Upstream Synthesis Route

[1]ChemicalCommunications,2009,#20,p.2848-2850

[2]BulletinoftheChemicalSocietyofJapan,2015,vol.88,#6,p.784-791

[3]SyntheticCommunications,2005,vol.35,#24,p.3187-3190

[4]InorganicChemistry,2013,vol.52,#11,p.6481-6501

[5]AngewandteChemie-InternationalEdition,2017,vol.56,#23,p.6483-6487

[6]Angew.Chem.,2017,vol.129,#23,p.6583-6587,5

[7]Patent:WO2017/102934,2017,A1,.Locationinpatent:Page/Pagecolumn23

[8]Heterocycles,2000,vol.53,#4,p.797-804

[9]Patent:US2004/186114,2004,A1,.Locationinpatent:Page/Pagecolumn61;62;64

[10]Patent:US5891889,1999,A,

[1]Patent:WO2005/12323,2005,A2,.Locationinpatent:Page/Pagecolumn46

[2]JournalofMedicinalChemistry,1998,vol.41,#11,p.1777-1788

[3]Patent:EP1422228,2004,A1,.Locationinpatent:Page199

[1]Patent:US2009/82403,2009,A1,.Locationinpatent:Page/Pagecolumn99

[2]JournalofMedicinalChemistry,1983,vol.26,#2,p.218-222

[3]PharmaceuticalBulletin,1953,vol.1,p.293,296

[4]PharmaceuticalBulletin,1953,vol.1,p.293,296

[1]ChemicalandPharmaceuticalBulletin,2000,vol.48,#10,p.1514-1518

[2]Patent:US2007/105904,2007,A1,.Locationinpatent:Page/Pagecolumn98

[1]SyntheticCommunications,2005,vol.35,#24,p.3187-3190

[2]Patent:US2009/44345,2009,A1,

Downstream Synthesis Route

[1]ChemicalCommunications,2009,p.2848-2850

[2]AdvancedSynthesisandCatalysis,2019,vol.361,p.2262-2267

[3]InorganicChemistry,2013,vol.52,p.6481-6501

[4]Synthesis,1996,p.991-996

[5]Tetrahedron,1997,vol.53,p.8257-8268

[6]BulletinoftheChemicalSocietyofJapan,2015,vol.88,p.784-791

[7]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1957,vol.77,p.11,13    Chem.Abstr.,1957,p.8745

[8]Patent:WO2007/25307,2007,A2.Locationinpatent:Page/Pagecolumn306

[9]Patent:US2016/168139,2016,A1.Locationinpatent:Paragraph0983;0986;0987

[10]Patent:WO2008/106139,2008,A1.Locationinpatent:Page/Pagecolumn475

[11]EuropeanJournalofOrganicChemistry,2019,vol.2019,p.3190-3194

67-56-1   
4-chloro-1-methoxypyridin-1-iumtetrafluoroborate 
  63071-10-3 

[1]SyntheticCommunications,1989,vol.19,p.317-326

67-56-1   
4-chloro-N-ethoxypyridiniumtetrafluoroborate 
  63071-10-3 

[1]SyntheticCommunications,1989,vol.19,p.317-326

[1]JournalofMedicinalChemistry,1983,vol.26,p.218-222

[2]ChemicalandPharmaceuticalBulletin,2000,vol.48,p.1514-1518

[1]JournalofMedicinalChemistry,1983,vol.26,p.218-222

Literature

Title: On the mechanism of dimethylarginine dimethylaminohydrolase inactivation by 4-halopyridines.

Journal: Journal of the American Chemical Society 20110720

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SDS
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