6404-28-0,MFCD00037270
Catalog No.:AA00E977

6404-28-0 | Boc-NLe-OH

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$8.00   $6.00
- +
5g
95%
in stock  
$39.00   $27.00
- +
25g
95%
in stock  
$105.00   $74.00
- +
100g
95%
in stock  
$386.00   $270.00
- +
500g
95%
in stock  
$1,886.00 $1,320.00
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00E977
Chemical Name:
Boc-NLe-OH
CAS Number:
6404-28-0
Molecular Formula:
C11H21NO4
Molecular Weight:
231.2887
MDL Number:
MFCD00037270
SMILES:
CCCC[C@@H](C(=O)O)NC(=O)OC(C)(C)C C11H21NO4
Properties
Properties
 
BP:
362.1°C at 760 mmHg  
Form:
Solid  
Refractive Index:
1.4425  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
245  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
7  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2.4  

Upstream Synthesis Route

[1]BioorganicandMedicinalChemistry,2015,vol.23,#21,p.6891-6899

[2]Bioorganicandmedicinalchemistryletters,2004,vol.14,#1,p.275-278

[1]TetrahedronLetters,1987,vol.28,#48,p.6069-6072

[1]BioorganicandMedicinalChemistryLetters,2005,vol.15,#17,p.3891-3895

[2]BioorganicandMedicinalChemistryLetters,2004,vol.14,#3,p.719-722

[1]TetrahedronAsymmetry,2006,vol.17,#13,p.1995-1999

[1]Organicletters,2001,vol.3,#6,p.897-899

Downstream Synthesis Route
37553-65-4    73821-95-1    6404-28-0    47355-10-2   
BocGlyOH,BocTyr(OdiClBzl)OH 
  141611-94-1 

[1]JournalofMedicinalChemistry,1992,vol.35,p.2806-2811

13734-34-4    73821-95-1    6404-28-0    47355-10-2   
BocSarOH,BocTyr(OdiClBzl)OH 
  141611-98-5 

[1]JournalofMedicinalChemistry,1992,vol.35,p.2806-2811

13734-34-4    6404-28-0    47355-10-2    155567-90-1   
BocGlyOH,BocTyr(OdiClBzl)OH,BocAsp(OcHx)OH 
  141611-95-2 

[1]JournalofMedicinalChemistry,1992,vol.35,p.2806-2811

13734-34-4    73821-95-1    6404-28-0    47355-10-2   
BocProOH,Boc(N-Me)Tyr(OdiClBzl)OH 
  141612-00-2 

[1]JournalofMedicinalChemistry,1992,vol.35,p.2806-2811

13734-34-4    73821-95-1    6404-28-0    47355-10-2   
BocProOH,BocTyr(OdiClBzl)OH 
  141611-99-6 

[1]JournalofMedicinalChemistry,1992,vol.35,p.2806-2811

Literature

Title: Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Journal: Nature chemical biology 20090101

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Additional Info:
SDS
Historical Records
Tags:6404-28-0 Molecular Formula|6404-28-0 MDL|6404-28-0 SMILES|6404-28-0 Boc-NLe-OH
Catalog No.: AA00E977
6404-28-0,MFCD00037270
6404-28-0 | Boc-NLe-OH
Pack Size: 1g
Purity: 95%
in stock
$8.00 $6.00
Pack Size: 5g
Purity: 95%
in stock
$39.00 $27.00
Pack Size: 25g
Purity: 95%
in stock
$105.00 $74.00
Pack Size: 100g
Purity: 95%
in stock
$386.00 $270.00
Pack Size: 500g
Purity: 95%
in stock
$1,886.00 $1,320.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00E977
Chemical Name: Boc-NLe-OH
CAS Number: 6404-28-0
Molecular Formula: C11H21NO4
Molecular Weight: 231.2887
MDL Number: MFCD00037270
SMILES: CCCC[C@@H](C(=O)O)NC(=O)OC(C)(C)C C11H21NO4
Properties
BP: 362.1°C at 760 mmHg  
Form: Solid  
Refractive Index: 1.4425  
Storage: Keep in dry area;Room Temperature;  
Complexity: 245  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 7  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2.4  
Upstream Synthesis Route
327-57-1    24424-99-5    6404-28-0 

[1]BioorganicandMedicinalChemistry,2015,vol.23,#21,p.6891-6899

[2]Bioorganicandmedicinalchemistryletters,2004,vol.14,#1,p.275-278

116640-17-6    6404-28-0 

[1]TetrahedronLetters,1987,vol.28,#48,p.6069-6072

87974-77-4    6404-28-0 

[1]BioorganicandMedicinalChemistryLetters,2005,vol.15,#17,p.3891-3895

[2]BioorganicandMedicinalChemistryLetters,2004,vol.14,#3,p.719-722

145618-64-0    6404-28-0    116611-59-7 

[1]TetrahedronAsymmetry,2006,vol.17,#13,p.1995-1999

335628-17-6    6404-28-0 

[1]Organicletters,2001,vol.3,#6,p.897-899

Downstream Synthesis Route
37553-65-4    73821-95-1    6404-28-0    47355-10-2   
BocGlyOH,BocTyr(OdiClBzl)OH 
  141611-94-1 

[1]JournalofMedicinalChemistry,1992,vol.35,p.2806-2811

13734-34-4    73821-95-1    6404-28-0    47355-10-2   
BocSarOH,BocTyr(OdiClBzl)OH 
  141611-98-5 

[1]JournalofMedicinalChemistry,1992,vol.35,p.2806-2811

13734-34-4    6404-28-0    47355-10-2    155567-90-1   
BocGlyOH,BocTyr(OdiClBzl)OH,BocAsp(OcHx)OH 
  141611-95-2 

[1]JournalofMedicinalChemistry,1992,vol.35,p.2806-2811

13734-34-4    73821-95-1    6404-28-0    47355-10-2   
BocProOH,Boc(N-Me)Tyr(OdiClBzl)OH 
  141612-00-2 

[1]JournalofMedicinalChemistry,1992,vol.35,p.2806-2811

13734-34-4    73821-95-1    6404-28-0    47355-10-2   
BocProOH,BocTyr(OdiClBzl)OH 
  141611-99-6 

[1]JournalofMedicinalChemistry,1992,vol.35,p.2806-2811

Literature fold

Title: Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Journal: Nature chemical biology20090101

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