+1 858-523-8231
Login | Register
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
Home Other Building Blocks 1522-13-0
1522-13-0,MFCD00004449
Catalog No.:AA003D3W

1522-13-0 | 1,1,3-Triphenylpropargyl alcohol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$15.00   $11.00
- +
1g
97%
in stock  
$27.00   $19.00
- +
5g
>98.0%(GC)
in stock  
$48.00   $34.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003D3W
Chemical Name:
1,1,3-Triphenylpropargyl alcohol
CAS Number:
1522-13-0
Molecular Formula:
C21H16O
Molecular Weight:
284.3511
MDL Number:
MFCD00004449
SMILES:
OC(c1ccccc1)(c1ccccc1)C#Cc1ccccc1
NSC Number:
52241
Properties
Properties
 
BP:
470.7°C at 760 mmHg  
Form:
Solid  
MP:
80-82 °C(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
376  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
4  
XLogP3:
4.6  

Downstream Synthesis Route

[1]JournaloftheChemicalSociety.Chemicalcommunications,1989,p.386-387

[2]InorganicChemistry,2013,vol.52,p.6533-6542

[3]Patent:CN105503553,2016,A.Locationinpatent:Paragraph0087;0088;0089;0090;0091;0092;0093;0094

[4]Patent:CN110078611,2019,A.Locationinpatent:Paragraph0014-0019

[5]Synthesis,2017,vol.49,p.3149-3156

[6]BulletinoftheChemicalSocietyofJapan,1992,vol.65,p.2594-2598

[7]TetrahedronLetters,2009,vol.50,p.4773-4776

[8]OrganicLetters,2006,vol.8,p.4027-4029

[9]SyntheticCommunications,2014,vol.44,p.1924-1929

[10]Chemistry-AEuropeanJournal,2012,vol.18,p.4748-4758

[11]CatalysisLetters,2020,vol.150,p.2132-2139

[12]JournaloftheAmericanChemicalSociety,2002,vol.124,p.15172-15173

[13]EuropeanJournalofOrganicChemistry,2011,p.5967-5970

[14]JournalofOrganicChemistry,2019,vol.84,p.4246-4262

[15]ChemischeBerichte,1922,vol.55,p.817

[16]ChemischeBerichte,1922,vol.55,p.817

[17]BulletindelaSocieteChimiquedeFrance,1923,vol.<4>33,p.935,938

[18]BulletindelaSocieteChimiquedeFrance,1923,vol.<4>33,p.935,938

[19]BulletindelaSocieteChimiquedeFrance,1924,vol.<4>35,p.1421,1422

[20]JustusLiebigsAnnalenderChemie,1923,vol.433,p.257

[21]ChemischeBerichte,1922,vol.55,p.817

[22]ChemischeBerichte,1922,vol.55,p.817

[23]ChemischeBerichte,1922,vol.55,p.817

[24]JournaloftheChemicalSociety,1924,vol.125,p.843

[25]JournaloftheChemicalSociety,1963,p.2707-2711

[26]TetrahedronLetters,1996,vol.37,p.853-856

[27]Chemistry-AEuropeanJournal,2010,vol.16,p.9555-9562

[28]Chemistry-AEuropeanJournal,2012,vol.18,p.11894-11898

[29]AngewandteChemie-InternationalEdition,2015,vol.54,p.5658-5661    Angew.Chem.,2015,vol.127,p.45750-45753    AngewandteChemie,2015,vol.127,p.45750-45753

[30]JournaloftheAmericanChemicalSociety,2016,vol.138,p.13408-13414

[31]OrganicLetters,2018,vol.20,p.5573-5577

[1]EuropeanJournalofMedicinalChemistry,2012,vol.54,p.483-498

[2]ZhurnalRusskagoFiziko-KhimicheskagoObshchestva,1920,vol.50,p.23    ChemischesZentralblatt,1923,vol.94,p.1391

[1]TetrahedronLetters,2012,vol.53,p.2160-2163

[2]OrganicLetters,2013,vol.15,p.5222-5225

[3]AdvancedSynthesisandCatalysis,2018,vol.360,p.4422-4428

[4]EuropeanJournalofOrganicChemistry,2017,vol.2017,p.3381-3385

[5]JournalofChemicalSciences,2014,vol.126,p.1081-1089

[6]Patent:CN106632434,2017,A.Locationinpatent:Paragraph0056-0057

[7]ResearchonChemicalIntermediates,2013,vol.39,p.2391-2399

[8]TetrahedronLetters,2019,vol.60,p.2030-2034

[9]JournalofChemicalResearch,2007,p.370-372

[10]RussianJournalofOrganicChemistry,2007,vol.43,p.784-786

[11]MonatsheftefurChemie,1967,vol.98,p.1274-1309

[12]JournaloftheAmericanChemicalSociety,1965,vol.87,p.5632-5637

[13]EuropeanJournalofOrganicChemistry,2006,p.1383-1386

[14]Synlett,2005,p.2219-2223

[15]OrganicLetters,2006,vol.8,p.4027-4029

[16]OrganicLetters,2009,vol.11,p.4990-4993

[17]OrganicandBiomolecularChemistry,2010,vol.8,p.4016-4025

[18]JournalofOrganicChemistry,2010,vol.75,p.6290-6293

[19]JournalofOrganometallicChemistry,2011,vol.696,p.331-337

[20]OrganicLetters,2011,vol.13,p.3553-3555

[21]Chemistry-AEuropeanJournal,2012,vol.18,p.11894-11898

[22]JournalofOrganicChemistry,2014,vol.79,p.7616-7625

[23]Chemistry-AEuropeanJournal,2014,vol.20,p.12046-12050

[24]JournaloftheAmericanChemicalSociety,2016,vol.138,p.13408-13414

[25]JournaloftheAmericanChemicalSociety,2017,vol.139,p.6526-6529

[26]AdvancedSynthesisandCatalysis,2017,vol.359,p.2735-2740

[27]TetrahedronLetters,2017,vol.58,p.4642-4647

[28]AdvancedSynthesisandCatalysis,2018,vol.360,p.870-874

[29]AdvancedSynthesisandCatalysis,2018,vol.360,p.2796-2800

[30]JournalofOrganicChemistry,2018,vol.83,p.15043-15056

[31]OrganicandBiomolecularChemistry,2019,vol.17,p.1924-1928

[32]EuropeanJournalofOrganicChemistry,2019,vol.2019,p.5740-5748

[33]Advancedsynthesisandcatalysis,2020

[34]EuropeanJournalofOrganicChemistry,2020

1522-13-0    135-19-3   
1,3,3-triphenyl-3H-naphtho2,1-bpyran 

[1]JournalofChemicalSciences,2014,vol.126,p.1081-1089

[2]Synthesis,2011,p.3152-3160

[3]HelveticaChimicaActa,1997,vol.80,p.725-738

[4]TetrahedronLetters,2017,vol.58,p.4642-4647

86-56-6    1522-13-0   
dimethyl-(4-triphenylpropa-1,2-dienyl-naphthalen-1-yl)-amine 

[1]Karunakar,GallaV.;Periasamy,Mariappan[JournalofOrganicChemistry,2006,vol.71,#19,p.7463-7466]

Literature

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 1522-13-0
1517-69-7

1517-69-7

 1517-72-2

1517-72-2

 7228-47-9

7228-47-9

 617-94-7

617-94-7

 885-77-8

885-77-8

 1517-63-1

1517-63-1
Building Blocks
More >
Tags:1522-13-0 Molecular Formula|1522-13-0 MDL|1522-13-0 SMILES|1522-13-0 1,1,3-Triphenylpropargyl alcohol