203866-15-3,MFCD03094917
Catalog No.:AA00292X

203866-15-3 | N-Boc-4,4-difluoro-l-proline

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$16.00   $11.00
- +
5g
95%
in stock  
$38.00   $27.00
- +
10g
95%
in stock  
$69.00   $48.00
- +
25g
95%
in stock  
$158.00   $110.00
- +
50g
95%
in stock  
$308.00   $216.00
- +
100g
95%
in stock  
$553.00   $387.00
- +
250g
95%
in stock  
$1,229.00   $861.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00292X
Chemical Name:
N-Boc-4,4-difluoro-l-proline
CAS Number:
203866-15-3
Molecular Formula:
C10H15F2NO4
Molecular Weight:
251.2272
MDL Number:
MFCD03094917
SMILES:
O=C(N1CC(C[C@H]1C(=O)O)(F)F)OC(C)(C)C
Properties
Properties
 
BP:
340.4°C at 760 mmHg  
Form:
Solid  
MP:
120-124°C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
338  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.5  

Upstream Synthesis Route

[1]Patent:US2008/9497,2008,A1,.Locationinpatent:Page/Pagecolumn109

[2]Patent:WO2014/82379,2014,A1,.Locationinpatent:Page/Pagecolumn158;159;163

[3]TetrahedronLetters,1998,vol.39,#10,p.1169-1172

[1]BioorganicandMedicinalChemistryLetters,2009,vol.19,#14,p.3859-3862

[1]Patent:WO2012/146666,2012,A1,.Locationinpatent:Page/Pagecolumn138-139

[2]TetrahedronLetters,1998,vol.39,#10,p.1169-1172

[3]Patent:WO2014/19344,2014,A1,.Locationinpatent:Paragraph00451

[4]Patent:WO2014/82380,2014,A1,.Locationinpatent:Paragraph00427;00430

[5]Patent:WO2014/82379,2014,A1,.Locationinpatent:Page/Pagecolumn158;159;161

[6]Patent:WO2014/131315,2014,A1,.Locationinpatent:Page/Pagecolumn124;125

[7]Patent:US2015/79028,2015,A1,.Locationinpatent:Paragraph1117;1124;1125;1126;1127

[8]Patent:CN103880823,2017,B,.Locationinpatent:Paragraph1612;1627;1628

[9]BioorganicandMedicinalChemistry,2006,vol.14,#8,p.2725-2746

[10]Patent:US2014/357650,2014,A1,.Locationinpatent:Paragraph0281;0290;0291;0292;0293

[11]Patent:WO2005/23762,2005,A1,.Locationinpatent:Page/Pagecolumn72

[12]Patent:EP1659121,2006,A1,.Locationinpatent:Page/Pagecolumn19-20

[13]Patent:WO2004/99185,2004,A1,.Locationinpatent:Page48

[14]Patent:US2005/131019,2005,A1,.Locationinpatent:Page/Pagecolumn31;34

[15]Patent:WO2013/107820,2013,A1,.Locationinpatent:Page/Pagecolumn45

[16]JournalofMedicinalChemistry,2014,vol.57,#7,p.3053-3074

[17]Patent:WO2015/28095,2015,A1,.Locationinpatent:Paragraph00222

[18]Patent:US2016/297830,2016,A1,.Locationinpatent:Paragraph0303

[1]BioorganicandMedicinalChemistry,2006,vol.14,#8,p.2725-2746

[2]TetrahedronLetters,1998,vol.39,#10,p.1169-1172

[3]Patent:WO2013/107820,2013,A1,

[4]Patent:WO2014/19344,2014,A1,

[5]JournalofMedicinalChemistry,2014,vol.57,#7,p.3053-3074

[6]Patent:WO2014/82380,2014,A1,

[7]Patent:WO2014/82379,2014,A1,

[8]Patent:WO2014/131315,2014,A1,

[9]Patent:US2014/357650,2014,A1,

[10]Patent:US2015/79028,2015,A1,

[11]Patent:CN103880823,2017,B,

[1]BioorganicandMedicinalChemistry,2006,vol.14,#8,p.2725-2746

[2]TetrahedronLetters,1998,vol.39,#10,p.1169-1172

[3]JournalofMedicinalChemistry,2014,vol.57,#7,p.3053-3074

[4]Patent:WO2014/131315,2014,A1,

Downstream Synthesis Route

[1]BioorganicandMedicinalChemistry,2006,vol.14,p.2725-2746

[1]BioorganicandMedicinalChemistry,2006,vol.14,p.6900-6916

[1]BioorganicandMedicinalChemistry,2006,vol.14,p.6900-6916

[1]Patent:US2011/82165,2011,A1.Locationinpatent:Page/Pagecolumn29-30

[2]ChemicalCommunications,2011,vol.47,p.10040-10042

[3]Patent:US2011/105520,2011,A1.Locationinpatent:Page/Pagecolumn36

[4]ChemMedChem,2015,vol.10,p.1071-1078

[5]Patent:WO2014/19344,2014,A1.Locationinpatent:Paragraph00452

[6]Patent:WO2014/131315,2014,A1.Locationinpatent:Page/Pagecolumn125

[7]Patent:US2015/79028,2015,A1.Locationinpatent:Paragraph1117;1128;1129;1130

[8]Patent:CN103880823,2017,B.Locationinpatent:Paragraph1612;1631;1632

[9]Patent:WO2013/152198,2013,A1.Locationinpatent:Paragraph00463;00464

[10]ChemicalandPharmaceuticalBulletin,2006,vol.54,p.1515-1529

[11]Patent:WO2011/88045,2011,A1.Locationinpatent:Page/Pagecolumn161

[12]BioorganicandMedicinalChemistryLetters,2011,vol.21,p.5296-5300

[13]Patent:WO2015/109109,2015,A1

[14]Patent:US2017/44182,2017,A1

[1]ChemicalandPharmaceuticalBulletin,2006,vol.54,p.1515-1529

Literature
Quotation Request
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Additional Info:
SDS
Tags:203866-15-3 Molecular Formula|203866-15-3 MDL|203866-15-3 SMILES|203866-15-3 N-Boc-4,4-difluoro-l-proline
Catalog No.: AA00292X
203866-15-3,MFCD03094917
203866-15-3 | N-Boc-4,4-difluoro-l-proline
Pack Size: 1g
Purity: 97%
in stock
$16.00 $11.00
Pack Size: 5g
Purity: 95%
in stock
$38.00 $27.00
Pack Size: 10g
Purity: 95%
in stock
$69.00 $48.00
Pack Size: 25g
Purity: 95%
in stock
$158.00 $110.00
Pack Size: 50g
Purity: 95%
in stock
$308.00 $216.00
Pack Size: 100g
Purity: 95%
in stock
$553.00 $387.00
Pack Size: 250g
Purity: 95%
in stock
$1,229.00 $861.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00292X
Chemical Name: N-Boc-4,4-difluoro-l-proline
CAS Number: 203866-15-3
Molecular Formula: C10H15F2NO4
Molecular Weight: 251.2272
MDL Number: MFCD03094917
SMILES: O=C(N1CC(C[C@H]1C(=O)O)(F)F)OC(C)(C)C
Properties
BP: 340.4°C at 760 mmHg  
Form: Solid  
MP: 120-124°C  
Storage: Keep in dry area;Room Temperature;  
Complexity: 338  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 6  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.5  
Upstream Synthesis Route
203866-15-3    52683-81-5 

[1]Patent:US2008/9497,2008,A1,.Locationinpatent:Page/Pagecolumn109

[2]Patent:WO2014/82379,2014,A1,.Locationinpatent:Page/Pagecolumn158;159;163

[3]TetrahedronLetters,1998,vol.39,#10,p.1169-1172

67-56-1    203866-15-3    156046-05-8 

[1]BioorganicandMedicinalChemistryLetters,2009,vol.19,#14,p.3859-3862

203866-17-5    203866-15-3 

[1]Patent:WO2012/146666,2012,A1,.Locationinpatent:Page/Pagecolumn138-139

[2]TetrahedronLetters,1998,vol.39,#10,p.1169-1172

[3]Patent:WO2014/19344,2014,A1,.Locationinpatent:Paragraph00451

[4]Patent:WO2014/82380,2014,A1,.Locationinpatent:Paragraph00427;00430

[5]Patent:WO2014/82379,2014,A1,.Locationinpatent:Page/Pagecolumn158;159;161

[6]Patent:WO2014/131315,2014,A1,.Locationinpatent:Page/Pagecolumn124;125

[7]Patent:US2015/79028,2015,A1,.Locationinpatent:Paragraph1117;1124;1125;1126;1127

[8]Patent:CN103880823,2017,B,.Locationinpatent:Paragraph1612;1627;1628

[9]BioorganicandMedicinalChemistry,2006,vol.14,#8,p.2725-2746

[10]Patent:US2014/357650,2014,A1,.Locationinpatent:Paragraph0281;0290;0291;0292;0293

[11]Patent:WO2005/23762,2005,A1,.Locationinpatent:Page/Pagecolumn72

[12]Patent:EP1659121,2006,A1,.Locationinpatent:Page/Pagecolumn19-20

[13]Patent:WO2004/99185,2004,A1,.Locationinpatent:Page48

[14]Patent:US2005/131019,2005,A1,.Locationinpatent:Page/Pagecolumn31;34

[15]Patent:WO2013/107820,2013,A1,.Locationinpatent:Page/Pagecolumn45

[16]JournalofMedicinalChemistry,2014,vol.57,#7,p.3053-3074

[17]Patent:WO2015/28095,2015,A1,.Locationinpatent:Paragraph00222

[18]Patent:US2016/297830,2016,A1,.Locationinpatent:Paragraph0303

102195-80-2    203866-15-3 

[1]BioorganicandMedicinalChemistry,2006,vol.14,#8,p.2725-2746

[2]TetrahedronLetters,1998,vol.39,#10,p.1169-1172

[3]Patent:WO2013/107820,2013,A1,

[4]Patent:WO2014/19344,2014,A1,

[5]JournalofMedicinalChemistry,2014,vol.57,#7,p.3053-3074

[6]Patent:WO2014/82380,2014,A1,

[7]Patent:WO2014/82379,2014,A1,

[8]Patent:WO2014/131315,2014,A1,

[9]Patent:US2014/357650,2014,A1,

[10]Patent:US2015/79028,2015,A1,

[11]Patent:CN103880823,2017,B,

74844-91-0    203866-15-3 

[1]BioorganicandMedicinalChemistry,2006,vol.14,#8,p.2725-2746

[2]TetrahedronLetters,1998,vol.39,#10,p.1169-1172

[3]JournalofMedicinalChemistry,2014,vol.57,#7,p.3053-3074

[4]Patent:WO2014/131315,2014,A1,

Downstream Synthesis Route
40004-08-8    203866-15-3    886447-88-7 

[1]BioorganicandMedicinalChemistry,2006,vol.14,p.2725-2746

203866-15-3    449756-95-0    681128-16-5 

[1]BioorganicandMedicinalChemistry,2006,vol.14,p.6900-6916

203866-15-3    404922-72-1    911831-66-8 

[1]BioorganicandMedicinalChemistry,2006,vol.14,p.6900-6916

203866-15-3    215918-21-1 

[1]Patent:US2011/82165,2011,A1.Locationinpatent:Page/Pagecolumn29-30

[2]ChemicalCommunications,2011,vol.47,p.10040-10042

[3]Patent:US2011/105520,2011,A1.Locationinpatent:Page/Pagecolumn36

[4]ChemMedChem,2015,vol.10,p.1071-1078

[5]Patent:WO2014/19344,2014,A1.Locationinpatent:Paragraph00452

[6]Patent:WO2014/131315,2014,A1.Locationinpatent:Page/Pagecolumn125

[7]Patent:US2015/79028,2015,A1.Locationinpatent:Paragraph1117;1128;1129;1130

[8]Patent:CN103880823,2017,B.Locationinpatent:Paragraph1612;1631;1632

[9]Patent:WO2013/152198,2013,A1.Locationinpatent:Paragraph00463;00464

[10]ChemicalandPharmaceuticalBulletin,2006,vol.54,p.1515-1529

[11]Patent:WO2011/88045,2011,A1.Locationinpatent:Page/Pagecolumn161

[12]BioorganicandMedicinalChemistryLetters,2011,vol.21,p.5296-5300

[13]Patent:WO2015/109109,2015,A1

[14]Patent:US2017/44182,2017,A1

203866-15-3    317357-75-8 

[1]ChemicalandPharmaceuticalBulletin,2006,vol.54,p.1515-1529

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