7782-26-5,MFCD00063140
Catalog No.:AA003C08

7782-26-5 | (R)-(-)-2-Phenylpropionic acid

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5g
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$24.00   $17.00
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10g
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25g
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003C08
Chemical Name:
(R)-(-)-2-Phenylpropionic acid
CAS Number:
7782-26-5
Molecular Formula:
C9H10O2
Molecular Weight:
150.1745
MDL Number:
MFCD00063140
SMILES:
C[C@H](c1ccccc1)C(=O)O
Properties
Properties
 
BP:
115°C at 760 mmHg  
Form:
Liquid  
MP:
29-30 °C(lit.)  
Refractive Index:
n20/D 1.523(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
137  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.9  

Downstream Synthesis Route

[1]BulletinoftheChemicalSocietyofJapan,1979,vol.52,p.3329-3336

[2]JournalofFluorineChemistry,1992,vol.59,p.225-232

[1]JournaloftheAmericanChemicalSociety,1998,vol.120,p.4209-4214

[2]JournalofBiologicalChemistry,1930,vol.88,p.27,57

[3]CollectionofCzechoslovakChemicalCommunications,1968,vol.33,p.1911-1916

[4]ChemistryLetters,1992,p.2261-2262

[5]GazzettaChimicaItaliana,1988,vol.118,p.457-464

[6]JournalofMedicinalChemistry,1994,vol.37,p.1704-1711

[7]JournalofChemicalResearch,Miniprint,1988,p.1701-1739

[8]JournalofMedicinalChemistry,2004,vol.47,p.1434-1447

[9]JournalofMedicinalChemistry,2006,vol.49,p.7247-7251

[10]OrganicandBiomolecularChemistry,2005,vol.3,p.4402-4411

[11]Phytochemistry,1992,vol.31,p.1649-1652

[12]JournalofOrganicChemistryUSSR(EnglishTranslation),1987,vol.23,p.2240-2245    ZhurnalOrganicheskoiKhimii,1987,vol.23,p.2538-2544

[13]JournaloftheChemicalSociety.PerkintransactionsII,1987,p.193-196

[14]JournalofOrganicChemistry,2007,vol.72,p.7551-7559

[15]JournalofAgriculturalandFoodChemistry,2008,vol.56,p.4120-4127

[16]TetrahedronLetters,2016,vol.57,p.2152-2157

[17]Patent:EP1870404,2007,A1.Locationinpatent:Page/Pagecolumn28;30-31

[18]JournalofMedicinalChemistry,2019,vol.62,p.4411-4425

[1]JournalofOrganicChemistry,1959,vol.24,p.108

[1]JournalofOrganicChemistry,2014,vol.79,p.11988-12003

[2]JournaloftheAmericanChemicalSociety,1952,vol.74,p.923,925

[3]TetrahedronLetters,1995,vol.36,p.9129-9132

[4]JournaloftheAmericanChemicalSociety,1998,vol.120,p.11832-11833

[5]JournalofOrganicChemistry,1999,vol.64,p.9704-9710

[6]Tetrahedron,2003,vol.59,p.7527-7533

[7]AngewandteChemie-InternationalEdition,2011,vol.50,p.9085-9088

[8]AngewandteChemie-InternationalEdition,2017,vol.56,p.1371-1375    Angew.Chem.,2017,vol.129,p.1391-1395,5

[1]JournalofOrganicChemistry,1987,vol.52,p.3174-3176

[2]JournalofOrganicChemistry,1980,vol.45,p.62-65

[3]JournalofOrganicChemistry,1982,vol.47,p.2722-2730

[4]JournalofOrganicChemistry,1982,vol.47,p.2722-2730

[5]JournalofOrganometallicChemistry,1992,vol.435,p.133-147

[6]TetrahedronAsymmetry,1997,vol.8,p.177-179

[7]JournalofOrganicChemistry,1996,vol.61,p.6244-6251

[8]JournalofOrganometallicChemistry,1992,vol.435,p.133-147

[9]TetrahedronAsymmetry,1997,vol.8,p.177-179

[10]JournalofOrganicChemistry,1996,vol.61,p.6244-6251

[11]EuropeanJournalofOrganicChemistry,2000,p.2885-2891

[12]TetrahedronLetters,2001,vol.42,p.9047-9050

[13]ChemicalCommunications,2002,p.1570-1571

[14]AdvancedSynthesisandCatalysis,2004,vol.346,p.1440-1444

[15]AdvancedSynthesisandCatalysis,2006,vol.348,p.2172-2182

[16]JournalofOrganicChemistry,2000,vol.65,p.2043-2047

[17]Patent:US6348620,2002,B1.Locationinpatent:Pagecolumn4,7

[18]JournalofCatalysis,2009,vol.262,p.57-64

[19]AdvancedSynthesisandCatalysis,2008,vol.350,p.2024-2032

[20]AdvancedSynthesisandCatalysis,2009,vol.351,p.2779-2786

[21]ChemicalCommunications,2010,vol.46,p.156-158

[22]Patent:US2010/99875,2010,A1.Locationinpatent:Page/Pagecolumn22

[23]OrganicandBiomolecularChemistry,2011,vol.9,p.5266-5271

[24]EuropeanJournalofOrganicChemistry,2012,p.6737-6744

[25]EuropeanJournalofOrganicChemistry,2015,vol.2015,p.2214-2225

[26]EuropeanJournalofOrganicChemistry,2015,vol.2015,p.2214-2225

[27]ChemCatChem,2015,vol.7,p.1302-1311

[28]JournalofOrganometallicChemistry,2015,vol.791,p.41-45

[29]OrganicLetters,2016,vol.18,p.2122-2125

[30]Patent:CN105384623,2016,A.Locationinpatent:Paragraph0094;0095

[31]ChemicalScience,2016,vol.7,p.6669-6673

Literature

Title: Challenges of crystal structure prediction of diastereomeric salt pairs.

Journal: The journal of physical chemistry. B 20050915

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Additional Info:
SDS
Tags:7782-26-5 Molecular Formula|7782-26-5 MDL|7782-26-5 SMILES|7782-26-5 (R)-(-)-2-Phenylpropionic acid
Catalog No.: AA003C08
7782-26-5,MFCD00063140
7782-26-5 | (R)-(-)-2-Phenylpropionic acid
Pack Size: 250mg
Purity: 98%
in stock
$6.00 $4.00
Pack Size: 1g
Purity: 98%
in stock
$7.00 $5.00
Pack Size: 5g
Purity: 98%
in stock
$24.00 $17.00
Pack Size: 10g
Purity: 98%
in stock
$46.00 $32.00
Pack Size: 25g
Purity: 98%
in stock
$105.00 $74.00
Pack Size: 100g
Purity: 98%
in stock
$419.00 $294.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003C08
Chemical Name: (R)-(-)-2-Phenylpropionic acid
CAS Number: 7782-26-5
Molecular Formula: C9H10O2
Molecular Weight: 150.1745
MDL Number: MFCD00063140
SMILES: C[C@H](c1ccccc1)C(=O)O
Properties
BP: 115°C at 760 mmHg  
Form: Liquid  
MP: 29-30 °C(lit.)  
Refractive Index: n20/D 1.523(lit.)  
Storage: Keep in dry area;Room Temperature;  
Complexity: 137  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.9  
Downstream Synthesis Route
186581-53-3    7782-26-5    2328-26-9 

[1]BulletinoftheChemicalSocietyofJapan,1979,vol.52,p.3329-3336

[2]JournalofFluorineChemistry,1992,vol.59,p.225-232

7782-26-5    36240-11-6 

[1]JournaloftheAmericanChemicalSociety,1998,vol.120,p.4209-4214

[2]JournalofBiologicalChemistry,1930,vol.88,p.27,57

[3]CollectionofCzechoslovakChemicalCommunications,1968,vol.33,p.1911-1916

[4]ChemistryLetters,1992,p.2261-2262

[5]GazzettaChimicaItaliana,1988,vol.118,p.457-464

[6]JournalofMedicinalChemistry,1994,vol.37,p.1704-1711

[7]JournalofChemicalResearch,Miniprint,1988,p.1701-1739

[8]JournalofMedicinalChemistry,2004,vol.47,p.1434-1447

[9]JournalofMedicinalChemistry,2006,vol.49,p.7247-7251

[10]OrganicandBiomolecularChemistry,2005,vol.3,p.4402-4411

[11]Phytochemistry,1992,vol.31,p.1649-1652

[12]JournalofOrganicChemistryUSSR(EnglishTranslation),1987,vol.23,p.2240-2245    ZhurnalOrganicheskoiKhimii,1987,vol.23,p.2538-2544

[13]JournaloftheChemicalSociety.PerkintransactionsII,1987,p.193-196

[14]JournalofOrganicChemistry,2007,vol.72,p.7551-7559

[15]JournalofAgriculturalandFoodChemistry,2008,vol.56,p.4120-4127

[16]TetrahedronLetters,2016,vol.57,p.2152-2157

[17]Patent:EP1870404,2007,A1.Locationinpatent:Page/Pagecolumn28;30-31

[18]JournalofMedicinalChemistry,2019,vol.62,p.4411-4425

7782-26-5    2328-26-9 

[1]JournalofOrganicChemistry,1959,vol.24,p.108

7782-26-5    1123-85-9 

[1]JournalofOrganicChemistry,2014,vol.79,p.11988-12003

[2]JournaloftheAmericanChemicalSociety,1952,vol.74,p.923,925

[3]TetrahedronLetters,1995,vol.36,p.9129-9132

[4]JournaloftheAmericanChemicalSociety,1998,vol.120,p.11832-11833

[5]JournalofOrganicChemistry,1999,vol.64,p.9704-9710

[6]Tetrahedron,2003,vol.59,p.7527-7533

[7]AngewandteChemie-InternationalEdition,2011,vol.50,p.9085-9088

[8]AngewandteChemie-InternationalEdition,2017,vol.56,p.1371-1375    Angew.Chem.,2017,vol.129,p.1391-1395,5

492-38-6    7782-24-3    7782-26-5 

[1]JournalofOrganicChemistry,1987,vol.52,p.3174-3176

[2]JournalofOrganicChemistry,1980,vol.45,p.62-65

[3]JournalofOrganicChemistry,1982,vol.47,p.2722-2730

[4]JournalofOrganicChemistry,1982,vol.47,p.2722-2730

[5]JournalofOrganometallicChemistry,1992,vol.435,p.133-147

[6]TetrahedronAsymmetry,1997,vol.8,p.177-179

[7]JournalofOrganicChemistry,1996,vol.61,p.6244-6251

[8]JournalofOrganometallicChemistry,1992,vol.435,p.133-147

[9]TetrahedronAsymmetry,1997,vol.8,p.177-179

[10]JournalofOrganicChemistry,1996,vol.61,p.6244-6251

[11]EuropeanJournalofOrganicChemistry,2000,p.2885-2891

[12]TetrahedronLetters,2001,vol.42,p.9047-9050

[13]ChemicalCommunications,2002,p.1570-1571

[14]AdvancedSynthesisandCatalysis,2004,vol.346,p.1440-1444

[15]AdvancedSynthesisandCatalysis,2006,vol.348,p.2172-2182

[16]JournalofOrganicChemistry,2000,vol.65,p.2043-2047

[17]Patent:US6348620,2002,B1.Locationinpatent:Pagecolumn4,7

[18]JournalofCatalysis,2009,vol.262,p.57-64

[19]AdvancedSynthesisandCatalysis,2008,vol.350,p.2024-2032

[20]AdvancedSynthesisandCatalysis,2009,vol.351,p.2779-2786

[21]ChemicalCommunications,2010,vol.46,p.156-158

[22]Patent:US2010/99875,2010,A1.Locationinpatent:Page/Pagecolumn22

[23]OrganicandBiomolecularChemistry,2011,vol.9,p.5266-5271

[24]EuropeanJournalofOrganicChemistry,2012,p.6737-6744

[25]EuropeanJournalofOrganicChemistry,2015,vol.2015,p.2214-2225

[26]EuropeanJournalofOrganicChemistry,2015,vol.2015,p.2214-2225

[27]ChemCatChem,2015,vol.7,p.1302-1311

[28]JournalofOrganometallicChemistry,2015,vol.791,p.41-45

[29]OrganicLetters,2016,vol.18,p.2122-2125

[30]Patent:CN105384623,2016,A.Locationinpatent:Paragraph0094;0095

[31]ChemicalScience,2016,vol.7,p.6669-6673

Literature fold

Title: Challenges of crystal structure prediction of diastereomeric salt pairs.

Journal: The journal of physical chemistry. B20050915

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