26782-71-8,MFCD00004265
Catalog No.:AA003PTI

26782-71-8 | D-tert-Leucine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$6.00   $4.00
- +
1g
97%
in stock  
$7.00   $5.00
- +
5g
97%
in stock  
$16.00   $11.00
- +
10g
97%
in stock  
$31.00   $22.00
- +
25g
97%
in stock  
$73.00   $51.00
- +
100g
97%
in stock  
$267.00   $187.00
- +
500g
97%
in stock  
$1,331.00   $932.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003PTI
Chemical Name:
D-tert-Leucine
CAS Number:
26782-71-8
Molecular Formula:
C6H13NO2
Molecular Weight:
131.1729
MDL Number:
MFCD00004265
SMILES:
N[C@H](C(C)(C)C)C(=O)O
Properties
Properties
 
Form:
Solid  
MP:
≥300 °C(lit.)  
Refractive Index:
9 ° (C=3, H2O)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
115  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-1.8  

Literature

Title: Asymmetric construction of spirocyclohexanonerhodanines catalyzed by simple diamine derived from chiral tert-leucine.

Journal: Chemical communications (Cambridge, England) 20120921

Title: Chiral recognition of α-amino acids by an optically active (2S,5S,8S,11S)-2,5,8,11-tetraethyl cyclen cobalt(III) complex.

Journal: Inorganic chemistry 20110103

Title: Total synthesis of the large non-ribosomal peptide polytheonamide B.

Journal: Nature chemistry 20100401

Title: Scaleable catalytic asymmetric Strecker syntheses of unnatural alpha-amino acids.

Journal: Nature 20091015

Title: The tert-butyl group in chemistry and biology.

Journal: Organic & biomolecular chemistry 20080807

Title: Effect of organic cosolvent on kinetic resolution of tert-leucine by penicillin G acylase from Kluyvera citrophila.

Journal: Bioprocess and biosystems engineering 20060401

Title: Preparation of optically pure tert-leucine by penicillin G acylase-catalyzed resolution.

Journal: Preparative biochemistry & biotechnology 20060101

Title: Preferred conformations of peptides containing tert-leucine, a sterically demanding, lipophilic alpha-amino acid with a quaternary side-chain Cbeta atom.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20050408

Title: Highly selective asymmetric acetate aldol reactions of an N-acetyl thiazolidinethione reagent.

Journal: Organic letters 20040108

Title: An efficient and selective enzymatic oxidation system for the synthesis of enantiomerically pure D-tert-leucine.

Journal: Organic letters 20031002

Title: Enzyme-assisted preparation of D-tert.-leucine.

Journal: Bioscience, biotechnology, and biochemistry 20010901

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SDS
Tags:26782-71-8 Molecular Formula|26782-71-8 MDL|26782-71-8 SMILES|26782-71-8 D-tert-Leucine
Catalog No.: AA003PTI
26782-71-8,MFCD00004265
26782-71-8 | D-tert-Leucine
Pack Size: 250mg
Purity: 97%
in stock
$6.00 $4.00
Pack Size: 1g
Purity: 97%
in stock
$7.00 $5.00
Pack Size: 5g
Purity: 97%
in stock
$16.00 $11.00
Pack Size: 10g
Purity: 97%
in stock
$31.00 $22.00
Pack Size: 25g
Purity: 97%
in stock
$73.00 $51.00
Pack Size: 100g
Purity: 97%
in stock
$267.00 $187.00
Pack Size: 500g
Purity: 97%
in stock
$1,331.00 $932.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003PTI
Chemical Name: D-tert-Leucine
CAS Number: 26782-71-8
Molecular Formula: C6H13NO2
Molecular Weight: 131.1729
MDL Number: MFCD00004265
SMILES: N[C@H](C(C)(C)C)C(=O)O
Properties
Form: Solid  
MP: ≥300 °C(lit.)  
Refractive Index: 9 ° (C=3, H2O)  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 115  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -1.8  
Literature fold

Title: Asymmetric construction of spirocyclohexanonerhodanines catalyzed by simple diamine derived from chiral tert-leucine.

Journal: Chemical communications (Cambridge, England)20120921

Title: Chiral recognition of α-amino acids by an optically active (2S,5S,8S,11S)-2,5,8,11-tetraethyl cyclen cobalt(III) complex.

Journal: Inorganic chemistry20110103

Title: Total synthesis of the large non-ribosomal peptide polytheonamide B.

Journal: Nature chemistry20100401

Title: Scaleable catalytic asymmetric Strecker syntheses of unnatural alpha-amino acids.

Journal: Nature20091015

Title: The tert-butyl group in chemistry and biology.

Journal: Organic & biomolecular chemistry20080807

Title: Effect of organic cosolvent on kinetic resolution of tert-leucine by penicillin G acylase from Kluyvera citrophila.

Journal: Bioprocess and biosystems engineering20060401

Title: Preparation of optically pure tert-leucine by penicillin G acylase-catalyzed resolution.

Journal: Preparative biochemistry & biotechnology20060101

Title: Preferred conformations of peptides containing tert-leucine, a sterically demanding, lipophilic alpha-amino acid with a quaternary side-chain Cbeta atom.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20050408

Title: Highly selective asymmetric acetate aldol reactions of an N-acetyl thiazolidinethione reagent.

Journal: Organic letters20040108

Title: An efficient and selective enzymatic oxidation system for the synthesis of enantiomerically pure D-tert-leucine.

Journal: Organic letters20031002

Title: Enzyme-assisted preparation of D-tert.-leucine.

Journal: Bioscience, biotechnology, and biochemistry20010901

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