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Home Deuterated Building Blocks 90365-74-5
90365-74-5,MFCD01073893
Catalog No.:AA003AVJ

90365-74-5 | (3S,4S)-1-Benzyl-3,4-pyrrolidindiol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%(GC)
in stock  
$24.00   $17.00
- +
1g
98%(GC)
in stock  
$56.00   $39.00
- +
5g
97%
in stock  
$61.00   $43.00
- +
10g
97%
in stock  
$113.00   $79.00
- +
25g
97%
in stock  
$251.00   $176.00
- +
  • 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:
AA003AVJ
Chemical Name:
(3S,4S)-1-Benzyl-3,4-pyrrolidindiol
CAS Number:
90365-74-5
Molecular Formula:
C11H15NO2
Molecular Weight:
193.2423
MDL Number:
MFCD01073893
SMILES:
O[C@H]1CN(C[C@@H]1O)Cc1ccccc1
Properties
Properties
 
BP:
356.2 °C at 760 mmHg  
Form:
Solid  
MP:
94-100 °C  
Refractive Index:
1.5041 (estimate)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
170  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
2  
XLogP3:
0.3  

Upstream Synthesis Route

[1]SyntheticCommunications,2008,vol.38,#14,p.2374-2384

[2]Patent:EP2390254,2011,A1,.Locationinpatent:Page/Pagecolumn86

[3]BioorganicandMedicinalChemistryLetters,1999,vol.9,#16,p.2385-2390

[4]AngewandteChemie,1984,vol.96,#6,p.425-426

[5]BioorganicandMedicinalChemistry,2007,vol.15,#12,p.3965-3973

[6]Tetrahedron,2007,vol.63,#5,p.1243-1253

[7]JournalofCarbohydrateChemistry,2000,vol.19,#4-5,p.585-601

[8]Patent:CN105693520,2016,A,.Locationinpatent:Paragraph0154;0155;0156;0157;0158;0159

[9]Patent:EP3067351,2016,A1,.Locationinpatent:Paragraph0073;0074

[10]Patent:CN108658947,2018,A,.Locationinpatent:Paragraph0093;0118;0130-0132

[11]BioorganicandMedicinalChemistryLetters,2017,vol.27,#12,p.2818-2823

[12]BioorganicandMedicinalChemistryLetters,2004,vol.14,#5,p.1265-1268

[13]Synthesis,2006,#2,p.247-256

[14]Patent:US2004/19065,2004,A1,.Locationinpatent:Page/Pagecolumn22

[15]Synthesis,2010,#5,p.791-796

[16]ChemicalResearchinToxicology,2010,vol.23,#1,p.118-133

[17]Patent:US2012/295874,2012,A1,.Locationinpatent:Page/Pagecolumn170

[1]Tetrahedron,2007,vol.63,#5,p.1243-1253

[2]AngewandteChemie,1984,vol.96,#6,p.425-426

[3]Patent:CN105693520,2016,A,.Locationinpatent:Paragraph0148;0149;0159;0151;0152;0153

[4]Patent:EP3067351,2016,A1,.Locationinpatent:Paragraph0071;0072

[5]ChemicalandPharmaceuticalBulletin,1991,vol.39,#9,p.2219-2224

[6]TetrahedronAsymmetry,1997,vol.8,#11,p.1861-1867

[7]Patent:CN106946744,2017,A,.Locationinpatent:Paragraph0083;0186-0187

[8]AngewandteChemie-InternationalEdition,1998,vol.37,#13-14,p.1846-1850

[9]JournalofOrganicChemistry,2000,vol.65,#6,p.1750-1757

[10]JournalofMedicinalChemistry,2017,vol.60,#3,p.957-971

[11]Synthesis,2010,#5,p.791-796

[12]Patent:WO2008/24725,2008,A1,.Locationinpatent:Page/Pagecolumn122-123

[13]SyntheticCommunications,2008,vol.38,#14,p.2374-2384

[14]Synlett,2009,#5,p.747-750

[15]Patent:US2012/295874,2012,A1,.Locationinpatent:Page/Pagecolumn169;170

[16]Patent:US2015/141402,2015,A1,.Locationinpatent:Paragraph0650;0651

[17]ChemischeBerichte,1986,vol.119,#11,p.3326-3343

[18]Heterocycles,1992,vol.34,#8,p.1519-1522

[19]JournalofOrganicChemistry,1996,vol.61,#23,p.8099-8102

[20]BioorganicandMedicinalChemistryLetters,1999,vol.9,#16,p.2385-2390

[21]BioorganicandMedicinalChemistryLetters,2004,vol.14,#5,p.1265-1268

[22]Patent:EP1577301,2005,A1,.Locationinpatent:Page/Pagecolumn162

[23]Patent:US5585500,1996,A,

[24]Patent:US2005/20645,2005,A1,

[25]Tetrahedron,2008,vol.64,#7,p.1197-1203

[26]Patent:EP1405852,2004,A1,.Locationinpatent:Page150

[27]ChemicalResearchinToxicology,2010,vol.23,#1,p.118-133

[28]BioorganicandMedicinalChemistryLetters,2011,vol.21,#6,p.1810-1814

[1]BioorganicandMedicinalChemistryLetters,2017,vol.27,#12,p.2818-2823

[1]SyntheticCommunications,2008,vol.38,#9,p.1365-1374

[1]Patent:US6090950,2000,A,

[2]CollectionofCzechoslovakChemicalCommunications,2012,vol.77,#3,p.224-233

Downstream Synthesis Route

[1]JournalofOrganicChemistry,1992,vol.57,p.1316-1318

[2]JournalofOrganicChemistry,1996,vol.61,p.8099-8102

[1]ChemicalandPharmaceuticalBulletin,1991,vol.39,p.2219-2224

[2]AdvancedSynthesisandCatalysis,2009,vol.351,p.1155-1161

[1]SyntheticCommunications,2008,vol.38,p.2374-2384

[2]Patent:EP2390254,2011,A1.Locationinpatent:Page/Pagecolumn86

[3]BioorganicandMedicinalChemistryLetters,1999,vol.9,p.2385-2390

[4]AngewandteChemie,1984,vol.96,p.425-426

[5]BioorganicandMedicinalChemistry,2007,vol.15,p.3965-3973

[6]Tetrahedron,2007,vol.63,p.1243-1253

[7]JournalofCarbohydrateChemistry,2000,vol.19,p.585-601

[8]Patent:CN105693520,2016,A.Locationinpatent:Paragraph0154;0155;0156;0157;0158;0159

[9]Patent:EP3067351,2016,A1.Locationinpatent:Paragraph0073;0074

[10]Patent:CN108658947,2018,A.Locationinpatent:Paragraph0093;0118;0130-0132

[11]BioorganicandMedicinalChemistryLetters,2017,vol.27,p.2818-2823

[12]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.1265-1268

[13]Synthesis,2006,p.247-256

[14]Patent:US2004/19065,2004,A1.Locationinpatent:Page/Pagecolumn22

[15]Synthesis,2010,p.791-796

[16]ChemicalResearchinToxicology,2010,vol.23,p.118-133

[17]Patent:US2012/295874,2012,A1.Locationinpatent:Page/Pagecolumn170

[1]BeilsteinJournalofOrganicChemistry,2012,vol.8,p.951-957

[2]TetrahedronAsymmetry,1996,vol.7,p.1659-1674

[3]ChemicalandPharmaceuticalBulletin,1991,vol.39,p.2219-2224

[1]SyntheticCommunications,2008,vol.38,p.2374-2384

[2]ChemischeBerichte,1986,vol.119,p.3326-3343

[3]Patent:CN106946744,2017,A.Locationinpatent:Paragraph0083;0188-0189

[4]Tetrahedron,2008,vol.64,p.1197-1203

[5]BioorganicandMedicinalChemistryLetters,2011,vol.21,p.1810-1814

[6]Patent:CN104725173,2017,B.Locationinpatent:Paragraph0076;0077

Literature
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SDS
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Tags:90365-74-5 Molecular Formula|90365-74-5 MDL|90365-74-5 SMILES|90365-74-5 (3S,4S)-1-Benzyl-3,4-pyrrolidindiol