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13623-25-1,MFCD00021232
Catalog No.:AA003N6H

13623-25-1 | 6-Methoxy-1-indanone

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  
$29.00   $21.00
- +
100g
98%
in stock  
$65.00   $46.00
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500g
98%
in stock  
$323.00   $226.00
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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:
AA003N6H
Chemical Name:
6-Methoxy-1-indanone
CAS Number:
13623-25-1
Molecular Formula:
C10H10O2
Molecular Weight:
162.1852
MDL Number:
MFCD00021232
SMILES:
COc1ccc2c(c1)C(=O)CC2
NSC Number:
338231
Properties
Properties
 
BP:
291.7°C at 760 mmHg  
Form:
Solid  
MP:
105-109 °C(lit.)  
Refractive Index:
1.6000 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
188  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
1.6  

Upstream Synthesis Route

[1]Synthesis(Germany),2018,vol.50,#24,p.4963-4981

[1]Molecules,2014,vol.19,#5,p.5599-5610

[2]ACSMedicinalChemistryLetters,2016,vol.7,#5,p.470-475

[3]OrganicandBiomolecularChemistry,2017,vol.15,#35,p.7374-7379

[4]SyntheticCommunications,1991,vol.21,#21,p.2231-2256

[5]TetrahedronLetters,2004,vol.45,#8,p.1741-1745

[6]ChemicalCommunications,2011,vol.47,#22,p.6290-6292

[7]JournaloftheAmericanChemicalSociety,1945,vol.67,p.1853

[8]JournaloftheAmericanChemicalSociety,1949,vol.71,p.1092,1095

[9]YakugakuZasshi,1956,vol.76,p.163,165,166

[10]Chem.Abstr.,1956,p.13850

[11]AngewandteChemie,1954,vol.66,p.435

[12]MonatsheftefuerChemie,1978,vol.109,p.405-419

[13]ChemischeBerichte,1969,vol.102,p.3656-3665

[14]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1984,#4,p.687-695

[15]Heterocycles,1988,vol.27,#9,p.2213-2217

[16]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1999,vol.38,#4,p.407-412

[17]Patent:US5569655,1996,A,

[18]EuropeanJournalofMedicinalChemistry,2010,vol.45,#1,p.25-37

[19]MolecularCrystalsandLiquidCrystals,2011,vol.545,p.149-155

[20]JournalofOrganicChemistry,2012,vol.77,#13,p.5788-5793

[21]Patent:US5554620,1996,A,

[1]JournalofOrganicChemistry,2012,vol.77,#13,p.5788-5793

[2]Patent:US2013/267712,2013,A1,.Locationinpatent:Paragraph0038-0039

[1]JournalofOrganicChemistry,1993,vol.58,#20,p.5386-5392

[1]TetrahedronLetters,1998,vol.39,#11,p.1385-1388

[2]Synthesis,1994,#9,p.915-916

[3]JournalofOrganicChemistry,1997,vol.62,#25,p.8767-8772

[4]EuropeanJournalofOrganicChemistry,2003,#3,p.578-586

[5]ChemCatChem,2013,vol.5,#1,p.126-129

Downstream Synthesis Route

[1]Li,Jinsi;Fang,Xuerong;Ming,Xin[JournalofOrganicChemistry,2020,vol.85,#7,p.4602-4610]

[2]Meth-Cohn,Otto;Moore,Clive;Rooyen,PetrusH.van[JournaloftheChemicalSociety.PerkintransactionsI,1985,p.1793-1802]

[3]CurrentPatentAssignee:FERRERINTERNACIONALSA-WO2009/53443,2009,A2Locationinpatent:Page/Pagecolumn11;20-21

[4]Peglion;Goument;Despaux;Charlot;Giraud;Nisole;Newman-Tancredi;Dekeyne;Bertrand;Genissel;Millan[JournalofMedicinalChemistry,2002,vol.45,#1,p.165-176]

[5]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-WO2009/5998,2009,A1Locationinpatent:Page/Pagecolumn260-261

[6]Locationinpatent:experimentalpartZhang,Rui;Dong,Jin;Xu,Yun-gen;Hua,Wei-yi;Wen,Na;You,Qi-dong[EuropeanJournalofMedicinalChemistry,2009,vol.44,#9,p.3771-3776]

[1]Lee,NamHo;Lee,Chang-Seob;Jung,Duk-Sang[TetrahedronLetters,1998,vol.39,#11,p.1385-1388]

[2]Zhao;Lee[Synthesis,1994,#9,p.915-916]

[3]Noureldin,NazihA.;Zhao,Dongyuan;Lee,DonaldG.[JournalofOrganicChemistry,1997,vol.62,#25,p.8767-8772]

[4]DeVondervoort,LizetteSchmieder-van;Bouttemy,Sabine;Heu,Ferdinand;Weissenboeck,Kurt;Alsters,PaulL.[EuropeanJournalofOrganicChemistry,2003,#3,p.578-586]

[5]Hsu,Shih-Fan;Plietker,Bernd[ChemCatChem,2013,vol.5,#1,p.126-129]

[1]JournalofOrganicChemistry,1984,vol.49,p.2517-2520

[2]JournalofOrganicChemistry,1970,vol.35,p.647-651

[3]MolecularCrystalsandLiquidCrystals,2011,vol.545,p.149-155

[4]JournalofMedicinalChemistry,2021,vol.64,p.1844-1855

[1]JournalofOrganicChemistry,1961,vol.26,p.4859-4866

[1]BioorganicandMedicinalChemistry,1999,vol.7,p.2801-2809

Literature

Title: Synthesis and evaluation of indatraline-based inhibitors for trypanothione reductase.

Journal: ChemMedChem 20110207

Title: A study on the conversion of indanones into carbostyrils.

Journal: Bioorganic & medicinal chemistry 20030515

Title: Interesting reaction of the indanone oximes under Beckmann rearrangement conditions.

Journal: Bioorganic & medicinal chemistry letters 20020211

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SDS
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