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16375-88-5,MFCD00016868
Catalog No.:AA001UAP

16375-88-5 | 4-Acetamidobenzyl alcohol

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Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$29.00   $21.00
- +
5g
98%
in stock  
$70.00   $49.00
- +
25g
98%
in stock  
$188.00   $132.00
- +
100g
98%
in stock  
$610.00   $427.00
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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:
AA001UAP
Chemical Name:
4-Acetamidobenzyl alcohol
CAS Number:
16375-88-5
Molecular Formula:
C9H11NO2
Molecular Weight:
165.1891
MDL Number:
MFCD00016868
SMILES:
OCc1ccc(cc1)NC(=O)C
Properties
Computed Properties
 
Complexity:
151  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
2  
XLogP3:
0.4  

Upstream Synthesis Route

[1]JournalofOrganicChemistry,1985,vol.50,#24,p.4884-4888

[1]JournalofOrganicChemistry,1985,vol.50,#24,p.4884-4888

[1]AdvancedSynthesisandCatalysis,2018,vol.360,#4,p.676-681

[2]ChemicalCommunications,2015,vol.51,#46,p.9567-9570

[3]OrganicLetters,2017,vol.19,#13,p.3656-3659

[4]CatalysisScienceandTechnology,2013,vol.3,#1,p.81-84

[5]Patent:US2007/149462,2007,A1,.Locationinpatent:Page/Pagecolumn22

[6]Patent:US9138442,2015,B2,.Locationinpatent:Page/Pagecolumn37

[7]ChemCatChem,2017,vol.9,#1,p.80-83

[8]Tetrahedron,1981,vol.37,p.2165-2172

[9]JournaloftheChemicalSociety,ChemicalCommunications,1981,#3,p.121-122

[10]TetrahedronLetters,2015,vol.56,#2,p.414-418

[11]Tetrahedron,2006,vol.62,#34,p.8164-8168

[12]Chemistry-AEuropeanJournal,2012,vol.18,#50,p.15935-15939

[13]AngewandteChemie-InternationalEdition,2013,vol.52,#19,p.5120-5124

[14]Angew.Chem.,2013,vol.125,#19,p.5224-5228

[1]ResearchonChemicalIntermediates,2017,vol.43,#1,p.413-422

[2]ChineseJournalofCatalysis,2014,vol.35,#3,p.368-375

[3]JournaloftheIranianChemicalSociety,2017,vol.14,#11,p.2467-2474

[4]AppliedCatalysisA:General,2010,vol.382,#2,p.293-302

[5]JournaloftheIranianChemicalSociety,2014,vol.11,#4,p.1103-1112

[6]JournalofOrganicChemistry,2001,vol.66,#26,p.8815-8830

[7]JournalofOrganicChemistry,2012,vol.77,#21,p.9553-9561

[8]JournalofOrganicChemistry,2018,vol.83,#5,p.2542-2553

[9]ChemistryofMaterials,2011,vol.23,#21,p.4844-4856

[10]JournaloftheAmericanChemicalSociety,2016,vol.138,#17,p.5568-5575

[1]ACSCatalysis,2016,vol.6,#3,p.1732-1736

Downstream Synthesis Route

[1]JournalofFluorineChemistry,1991,vol.54,p.268

[1]ChemicalandPharmaceuticalBulletin,1982,vol.30,p.2077-2086

[2]JournaloftheChemicalSociety,1963,p.1947-1954

[3]JournaloftheAmericanChemicalSociety,2016,vol.138,p.5568-5575

[1]JournaloftheAmericanChemicalSociety,1991,vol.113,p.5427-5434

[2]JournaloftheChemicalSociety,1963,p.1947-1954

[3]ChemicalandPharmaceuticalBulletin,1982,vol.30,p.2077-2086

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

[2]Tetrahedron,2015,vol.71,p.8725-8731

[3]SyntheticCommunications,2012,vol.42,p.2318-2326

[4]RSCAdvances,2015,vol.5,p.81415-81428

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

[6]JournalofOrganicChemistry,1988,vol.53,p.2154-2159

[7]BulletinoftheChemicalSocietyofJapan,1988,vol.61,p.1767-1772

[8]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1995,vol.34,p.968-974

[9]InternationalJournalofChemicalKinetics,1997,vol.29,p.9-16

[10]JournalofChemicalResearch,Miniprint,1998,p.2251-2272

[11]JournalofChemicalResearch,Miniprint,1999,p.2118-2135

[12]JournalofChemicalResearch,Miniprint,2001,p.562-585

[13]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,2000,vol.39,p.1258-1263

[14]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,2002,vol.41,p.493-499

[15]JournalofPhysicalOrganicChemistry,2002,vol.15,p.721-727

[16]JournaloftheIndianChemicalSociety,2004,vol.81,p.467-473

[17]JournalofChemicalResearch,2004,p.581-584

[18]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,2008,vol.47,p.669-676

[19]JournaloftheIndianChemicalSociety,2008,vol.85,p.496-501

[20]ChemistryofMaterials,2011,vol.23,p.4844-4856

[21]JournalofCatalysis,2017,vol.354,p.152-159

[1]AdvancedSynthesisandCatalysis,2018,vol.360,p.676-681

[2]ChemicalCommunications,2015,vol.51,p.9567-9570

[3]OrganicLetters,2017,vol.19,p.3656-3659

[4]Catalysisscienceandtechnology,2013,vol.3,p.81-84

[5]Patent:US2007/149462,2007,A1.Locationinpatent:Page/Pagecolumn22

[6]Patent:US9138442,2015,B2.Locationinpatent:Page/Pagecolumn37

[7]ChemCatChem,2017,vol.9,p.80-83

[8]Tetrahedron,1981,vol.37,p.2165-2172

[9]JournaloftheChemicalSociety.Chemicalcommunications,1981,p.121-122

[10]AdvancedSynthesisandCatalysis,2019,vol.361,p.786-790

[11]TetrahedronLetters,2015,vol.56,p.414-418

[12]Tetrahedron,2006,vol.62,p.8164-8168

[13]Chemistry-AEuropeanJournal,2012,vol.18,p.15935-15939

[14]AngewandteChemie-InternationalEdition,2013,vol.52,p.5120-5124    Angew.Chem.,2013,vol.125,p.5224-5228

Literature

Title: Metabolites of a blocked chloramphenicol producer.

Journal: Journal of natural products 20030101

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