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873-76-7,MFCD00004652
Catalog No.:AA003L43

873-76-7 | 4-Chlorobenzyl alcohol

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10g
98%
in stock  
$6.00   $4.00
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25g
98%
in stock  
$7.00   $5.00
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100g
98%
in stock  
$23.00   $16.00
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500g
98%
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$82.00   $57.00
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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:
AA003L43
Chemical Name:
4-Chlorobenzyl alcohol
CAS Number:
873-76-7
Molecular Formula:
C7H7ClO
Molecular Weight:
142.5829
MDL Number:
MFCD00004652
SMILES:
OCc1ccc(cc1)Cl
NSC Number:
5286
Properties
Properties
 
BP:
234°C at 760 mmHg  
Form:
Solid  
MP:
68-71 °C(lit.)  
Refractive Index:
1.5390 (estimate)  
Solubility:
2.5g/l  
Storage:
Keep in dry area;Room Temperature;  

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

Upstream Synthesis Route

[1]JournalofChemicalResearch,2017,vol.41,#1,p.25-29

[1]OrganicLetters,2002,vol.4,#12,p.2055-2058

[2]Tetrahedron,2008,vol.64,#7,p.1213-1217

[1]ChemCatChem,2018,vol.10,#9,p.1993-1997

[2]OrganicLetters,2014,vol.16,#2,p.484-487

[3]OrganicLetters,2014,vol.16,#17,p.4424-4427

[1]ChemicalandPharmaceuticalBulletin,1990,vol.38,#8,p.2097-2101

[2]ChemicalandPharmaceuticalBulletin,1990,vol.38,#8,p.2097-2101

[1]ChemicalandPharmaceuticalBulletin,1994,vol.42,#2,p.402-404

Downstream Synthesis Route

[1]MonatsheftefurChemie,2004,vol.135,p.1251-1255

[2]SyntheticCommunications,2004,vol.34,p.2959-2963

[3]Chemistry-AEuropeanJournal,2020,vol.26,p.10620-10625

[4]LettersinOrganicChemistry,2012,vol.9,p.598-603,6

[5]EuropeanJournalofOrganicChemistry,2005,p.755-758

[6]Phosphorus,SulfurandSiliconandtheRelatedElements,2011,vol.186,p.1470-1482

[7]BulletinoftheChemicalSocietyofEthiopia,2012,vol.26,p.305-309

[8]TetrahedronLetters,2016,vol.57,p.168-171

[9]ActaChimicaSlovenica,2015,vol.62,p.775-783

[10]Tetrahedron,2005,vol.61,p.5699-5704

[11]TetrahedronLetters,2006,vol.47,p.1771-1775

[12]TetrahedronLetters,2013,vol.54,p.6874-6877

[13]JournaloftheChemicalSociety,1926,p.220

[14]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1987,vol.26,p.68-70

[15]JournaloftheChemicalSociety.PerkintransactionsII,1991,p.2067-2080

[16]Synthesis,2002,p.479-482

[17]ScientiaPharmaceutica,2001,vol.69,p.329-350

[18]Patent:US5506261,1996,A

[19]Patent:US5616596,1997,A

[20]Patent:US5753679,1998,A

[21]TetrahedronLetters,2011,vol.52,p.13-16

[22]OrganicandBiomolecularChemistry,2013,vol.11,p.1463-1467

[23]ChemicalCommunications,2014,vol.50,p.3692-3694

[24]OrganicLetters,2014,vol.16,p.484-487

[25]OrganicLetters,2014,vol.16,p.4424-4427

[26]MedChemComm,2015,vol.6,p.1104-1116

[27]JournaloftheAmericanChemicalSociety,2015,vol.137,p.9567-9570

[28]OrganicandBiomolecularChemistry,2015,vol.13,p.10136-10149

[29]BioorganicandMedicinalChemistryLetters,2016,vol.26,p.561-569

[30]MedicinalChemistryResearch,2016,vol.25,p.790-804

[31]EuropeanJournalofMedicinalChemistry,2017,vol.127,p.100-114

[32]JournalofHeterocyclicChemistry,2017,vol.54,p.413-421

[33]AsianJournalofChemistry,2018,vol.30,p.651-654

[1]SyntheticCommunications,1990,vol.20,p.1843-1852

[1]JournalofOrganicChemistry,1993,vol.58,p.5643-5649

[1]Patent:WO2011/75537,2011,A1.Locationinpatent:Page/Pagecolumn80

[2]Patent:WO2018/98128,2018,A1.Locationinpatent:Paragraph0412

[3]ChemicalandPharmaceuticalBulletin,1990,vol.38,p.110-115

[4]JournalofMedicinalChemistry,2001,vol.44,p.4468-4474

[5]Patent:WO2016/196513,2016,A1.Locationinpatent:Paragraph0234

[1]Synthesis,1987,p.647-648

Literature

Title: S-benzylisothiourea derivatives as small-molecule inhibitors of indoleamine-2,3-dioxygenase.

Journal: Bioorganic & medicinal chemistry letters 20100901

Title: Hetero-seeding and solid mixture to obtain new crystalline forms.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20090101

Title: Oxidation of p-chlorotoluene and cyclohexene catalysed by polymer-anchored oxovanadium(IV) and copper(II) complexes of amino acid derived tridentate ligands.

Journal: Dalton transactions (Cambridge, England : 2003) 20080828

Title: Metabolism of 4,4'-dichlorobiphenyl by white-rot fungi Phanerochaete chrysosporium and Phanerochaete sp. MZ142.

Journal: Applied microbiology and biotechnology 20060901

Title: Mild and efficient oxidation of alcohols with sodium periodate catalyzed by polystyrene-bound Mn(III)porphyrin.

Journal: Bioorganic & medicinal chemistry 20050415

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