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1450-72-2,MFCD00002380
Catalog No.:AA001KDK

1450-72-2 | 2'-Hydroxy-5'-methylacetophenone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$9.00   $6.00
- +
5g
98%
in stock  
$20.00   $14.00
- +
10g
98%
in stock  
$33.00   $23.00
- +
25g
98%
in stock  
$55.00   $38.00
- +
100g
98%
in stock  
$173.00   $121.00
- +
  • 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:
AA001KDK
Chemical Name:
2'-Hydroxy-5'-methylacetophenone
CAS Number:
1450-72-2
Molecular Formula:
C9H10O2
Molecular Weight:
150.1745
MDL Number:
MFCD00002380
SMILES:
Cc1ccc(c(c1)C(=O)C)O
FEMA Number:
4594
Properties
Properties
 
BP:
210.0°C  
Form:
Solid  
MP:
45-48 °C  
Refractive Index:
1.5369 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
154  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2.3  

Upstream Synthesis Route

[1]CatalysisLetters,2015,vol.145,#3,p.939-946

[1]CatalysisLetters,2015,vol.145,#3,p.939-946

[1]JournalofOrganicChemistry,1981,vol.46,p.4971-4975

[2]JournalofChemicalResearch,Miniprint,2003,#12,p.1258-1270

[3]JournalofChemicalResearch,Synopses,1999,#9,p.574-575

[4]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1996,vol.35,#7,p.734-736

[5]JournalofChemicalResearch,Miniprint,1998,#10,p.2678-2695

[6]ChineseChemicalLetters,2016,vol.27,#7,p.1058-1063

[7]BulletindelaSocieteChimiquedeFrance,1987,#1,p.123-124

[8]Synthesis,1985,#9,p.901-902

[9]Synthesis,1982,#11,p.940-942

[10]IndianJournalofChemistry,SectionB:OrganicChemistryIncludingMedicinalChemistry,1994,vol.33,#2,p.184-185

[11]IndianJournalofChemistry,SectionB:OrganicChemistryIncludingMedicinalChemistry,1994,vol.33,#2,p.184-185

[12]EuropeanJournalofPharmacology,2005,vol.512,#2-3,p.97-104

[13]TetrahedronLetters,1996,vol.37,#42,p.7659-7660

[14]SyntheticCommunications,2004,vol.34,#8,p.1433-1440

[15]Heterocycles,2016,vol.93,#1,p.164-184

[16]Synthesis,2004,#11,p.1789-1792

[17]TetrahedronLetters,1996,vol.37,#12,p.2053-2056

[18]PharmacyandPharmacologyCommunications,1999,vol.5,#5,p.323-329

[19]OrganicLetters,2016,vol.18,#15,p.3766-3769

[20]ChemischeBerichte,1924,vol.57,p.92

[21]JustusLiebigsAnnalenderChemie,1926,vol.446,p.157Anm.2,177

[22]ChemischeBerichte,1921,vol.54,p.1533

[23]JustusLiebigsAnnalenderChemie,1928,vol.460,p.89

[24]JournaloftheChemicalSociety,1958,p.2926,2929

[25]JournaloftheChemicalSociety,1958,p.2926,2929

[26]JournaloftheChemicalSociety,1958,p.2926,2929

[27]JournaloftheChemicalSociety,1958,p.2926,2929

[28]JournaloftheChemicalSociety,1957,p.3016,3018

[29]JustusLiebigsAnnalenderChemie,1954,vol.587,p.1,15

[30]ChemischeBerichte,1939,vol.72,p.1414,1424

[31]JournaloftheChemicalSociety,PerkinTransactions2:PhysicalOrganicChemistry(1972-1999),1990,p.1893-1898

[32]Chemicalresearchintoxicology,2002,vol.15,#8,p.1106-1112

[33]BioorganicandMedicinalChemistry,2005,vol.13,#21,p.5996-6001

[34]JournalofMedicinalChemistry,2002,vol.45,#19,p.4188-4201

[35]Patent:US2011/98425,2011,A1,

[36]RussianJournalofPhysicalChemistryA,2010,vol.84,#12,p.2182-2186

[37]BioorganicandMedicinalChemistryLetters,2011,vol.21,#10,p.2855-2859

[38]AsianJournalofChemistry,2011,vol.23,#10,p.4616-4620

[39]OrientalJournalofChemistry,2011,vol.27,#3,p.1053-1062

[40]OrientalJournalofChemistry,2012,vol.28,#2,p.921-925,5

[41]MedicinalChemistryResearch,2018,vol.27,#8,p.1971-1983

[42]MedicinalChemistryResearch,2012,vol.21,#8,p.1833-1849,17

[43]BioorganicandMedicinalChemistry,2013,vol.21,#11,p.2826-2831

[44]EuropeanJournalofMedicinalChemistry,2013,vol.65,p.389-402

[45]EuropeanJournalofMedicinalChemistry,2015,vol.93,p.64-73

[46]MedChemComm,2013,vol.4,#9,p.1257-1266

[47]JournalofFluorineChemistry,2014,vol.160,p.77-81

[48]JournalofPhotochemistryandPhotobiologyA:Chemistry,2016,vol.329,p.238-245

[49]AsianJournalofChemistry,2017,vol.29,#1,p.119-123

[50]RussianJournalofOrganicChemistry,2017,vol.53,#3,p.459-461

[51]Zh.Org.Khim.,

[52]HeterocyclicCommunications,2017,vol.23,#4,p.325-330

[53]HeterocyclicCommunications,2018,vol.24,#1,p.59-65

[54]Patent:CN104803924,2017,B,.Locationinpatent:Paragraph0049;0054;0058

[1]JournaloftheChemicalSociety,DaltonTransactions:InorganicChemistry(1972-1999),1983,p.2429-2434

[2]ChemicalCommunications,2015,vol.51,#55,p.11060-11063

[3]Synthesis,2003,#18,p.2877-2881

[4]JournalfuerPraktischeChemie(Leipzig),1989,vol.331,#4,p.617-630

[5]Synthesis,1990,#12,p.1172-1173

[6]CanadianJournalofChemistry,1981,vol.59,p.2314-2327

[7]ChemistryofHeterocyclicCompounds,2004,vol.40,#5,p.635-640

[8]JournalofMedicinalChemistry,2007,vol.50,#9,p.2108-2116

[9]Patent:US2015/369812,2015,A1,.Locationinpatent:Paragraph0114

[10]ChemicalBiologyandDrugDesign,2017,vol.89,#1,p.141-151

[1]JournalofHeterocyclicChemistry,2014,vol.51,#2,p.291-302

[2]SyntheticCommunications,2014,vol.44,#7,p.929-935

Downstream Synthesis Route

[1]JournalofOrganicChemistry,1981,vol.46,p.4971-4975

[2]JournalofChemicalResearch,Miniprint,2003,p.1258-1270

[3]JournalofChemicalResearch-PartS,1999,p.574-575

[4]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1996,vol.35,p.734-736

[5]JournalofChemicalResearch,Miniprint,1998,p.2678-2695

[6]ChineseChemicalLetters,2016,vol.27,p.1058-1063

[7]BulletindelaSocieteChimiquedeFrance,1987,p.123-124

[8]Synthesis,1985,p.901-902

[9]Synthesis,1982,p.940-942

[10]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1994,vol.33,p.184-185

[11]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1994,vol.33,p.184-185

[12]EuropeanJournalofPharmacology,2005,vol.512,p.97-104

[13]TetrahedronLetters,1996,vol.37,p.7659-7660

[14]SyntheticCommunications,2004,vol.34,p.1433-1440

[15]Heterocycles,2016,vol.93,p.164-184

[16]Synthesis,2004,p.1789-1792

[17]LettersinOrganicChemistry,2018,vol.15,p.809-814

[18]TetrahedronLetters,1996,vol.37,p.2053-2056

[19]PharmacyandPharmacologyCommunications,1999,vol.5,p.323-329

[20]OrganicLetters,2016,vol.18,p.3766-3769

[21]ChemischeBerichte,1924,vol.57,p.92    JustusLiebigsAnnalenderChemie,1926,vol.446,p.157Anm.2,177

[22]JournaloftheChemicalSociety,1958,p.2926,2929

[23]JournaloftheChemicalSociety,1958,p.2926,2929

[24]JournaloftheChemicalSociety,1958,p.2926,2929

[25]JournaloftheChemicalSociety,1958,p.2926,2929

[26]JournaloftheChemicalSociety,1957,p.3016,3018

[27]JustusLiebigsAnnalenderChemie,1954,vol.587,p.1,15

[28]ChemischeBerichte,1939,vol.72,p.1414,1424

[29]JournaloftheChemicalSociety.PerkintransactionsII,1990,p.1893-1898

[30]Chemicalresearchintoxicology,2002,vol.15,p.1106-1112

[31]BioorganicandMedicinalChemistry,2005,vol.13,p.5996-6001

[32]JournalofMedicinalChemistry,2002,vol.45,p.4188-4201

[33]Patent:US2011/98425,2011,A1

[34]RussianJournalofPhysicalChemistry,2010,vol.84,p.2182-2186

[35]BioorganicandMedicinalChemistryLetters,2011,vol.21,p.2855-2859

[36]AsianJournalofChemistry,2011,vol.23,p.4616-4620

[37]OrientalJournalofChemistry,2011,vol.27,p.1053-1062

[38]OrientalJournalofChemistry,2012,vol.28,p.921-925,5

[39]MedicinalChemistryResearch,2012,vol.21,p.1833-1849,17

[40]BioorganicandMedicinalChemistry,2013,vol.21,p.2826-2831

[41]EuropeanJournalofMedicinalChemistry,2013,vol.65,p.389-402

[42]MedChemComm,2013,vol.4,p.1257-1266

[43]JournalofFluorineChemistry,2014,vol.160,p.77-81

[44]JournalofPhotochemistryandPhotobiologyA:Chemistry,2016,vol.329,p.238-245

[45]AsianJournalofChemistry,2017,vol.29,p.119-123

[46]RussianJournalofOrganicChemistry,2017,vol.53,p.459-461    Zh.Org.Khim.,

[47]HeterocyclicCommunications,2017,vol.23,p.325-330

[48]Patent:CN104803924,2017,B.Locationinpatent:Paragraph0049;0054;0058

[49]MedicinalChemistry,2020,vol.16,p.212-228

[50]BioorganicandMedicinalChemistryLetters,2020,vol.30

[1]JournalofChemicalResearch,2010,p.222-227

[2]BulletindelaSocieteChimiquedeFrance,1956,p.633,634

[3]BulletindelaSocieteChimiquedeFrance,1973,p.611-615

[1]JournaloftheAmericanChemicalSociety,1924,vol.46,p.1892

[1]Marathe[JournaloftheUniversityofPoona,ScienceandTechnology,1958,#14,p.63,66]

[1]JustusLiebigsAnnalenderChemie,1915,vol.408,p.247

[2]JournalofChemicalResearch,Miniprint,1989,p.1480-1500

[3]RussianJournalofOrganicChemistry,2017,vol.53,p.459-461    Zh.Org.Khim.,

[4]Patent:CN107337596,2017,A.Locationinpatent:Paragraph0026;0027;0031;0032

[5]MedicinalChemistryResearch,2018,vol.27,p.1971-1983

Literature

Title: Acaricidal toxicity of 2'-hydroxy-4'-methylacetophenone isolated from Angelicae koreana roots and structure-activity relationships of its derivatives.

Journal: Journal of agricultural and food chemistry 20120411

Title: [Analysis of volatile components of flowers of Fritillaria thunbergii by GC-TOF-MS].

Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20111001

Title: Molecular dynamics of cis-1-(2-hydroxy-5- methylphenyl)ethanone oxime and N-(2-hydroxy-4-methylphenyl)acetamide in solution studied by NMR spectroscopy.

Journal: Magnetic resonance in chemistry : MRC 20100901

Title: Bis{μ-2-(1H-indol-3-yl)-N'-[1-(5-methyl-2-oxidophen-yl)ethyl-idene]-aceto-hydraz-idato}bis-[aqua-zinc(II)] dimethyl sulfoxide tetra-solvate.

Journal: Acta crystallographica. Section E, Structure reports online 20080801

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