33105-81-6,MFCD00065933
Catalog No.:AA003PRT

33105-81-6 | DL-tert-leucine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$6.00   $4.00
- +
5g
97%
in stock  
$16.00   $11.00
- +
10g
97%
in stock  
$31.00   $22.00
- +
25g
98%
in stock  
$54.00   $38.00
- +
100g
98%
in stock  
$177.00 $124.00
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003PRT
Chemical Name:
DL-tert-leucine
CAS Number:
33105-81-6
Molecular Formula:
C6H13NO2
Molecular Weight:
131.1729
MDL Number:
MFCD00065933
SMILES:
NC(C(C)(C)C)C(=O)O
NSC Number:
203785
Properties
Properties
 
BP:
242.49°C (rough estimate)  
Form:
Solid  
MP:
>300 °C(lit.)  
Refractive Index:
1.4240 (estimate)  
Solubility:
H2O: 0.1 g/mL, clear, colorless  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
115  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
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:
1  
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: 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:33105-81-6 Molecular Formula|33105-81-6 MDL|33105-81-6 SMILES|33105-81-6 DL-tert-leucine
Catalog No.: AA003PRT
33105-81-6,MFCD00065933
33105-81-6 | DL-tert-leucine
Pack Size: 1g
Purity: 97%
in stock
$6.00 $4.00
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: 98%
in stock
$54.00 $38.00
Pack Size: 100g
Purity: 98%
in stock
$177.00 $124.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003PRT
Chemical Name: DL-tert-leucine
CAS Number: 33105-81-6
Molecular Formula: C6H13NO2
Molecular Weight: 131.1729
MDL Number: MFCD00065933
SMILES: NC(C(C)(C)C)C(=O)O
NSC Number: 203785
Properties
BP: 242.49°C (rough estimate)  
Form: Solid  
MP: >300 °C(lit.)  
Refractive Index: 1.4240 (estimate)  
Solubility: H2O: 0.1 g/mL, clear, colorless  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 115  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
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: 1  
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: 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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