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6456-74-2,MFCD00038194
Catalog No.:AA0038HK

6456-74-2 | tert-Butyl glycinate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$9.00   $6.00
- +
5g
95%
in stock  
$13.00   $9.00
- +
10g
97%
in stock  
$15.00   $11.00
- +
25g
97%
in stock  
$35.00   $25.00
- +
100g
95%
in stock  
$78.00   $54.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0038HK
Chemical Name:
tert-Butyl glycinate
CAS Number:
6456-74-2
Molecular Formula:
C6H13NO2
Molecular Weight:
131.1729
MDL Number:
MFCD00038194
SMILES:
NCC(=O)OC(C)(C)C
Properties
Computed Properties
 
Complexity:
104  
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:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.2  

Literature

Title: A powerful synergistic effect for highly efficient diastereo- and enantioselective phase-transfer catalyzed conjugate additions.

Journal: Chemical communications (Cambridge, England) 20110207

Title: Synthesis and structure-activity relationships of potent 1-(2-substituted-aminoacetyl)-4-fluoro-2-cyanopyrrolidine dipeptidyl peptidase IV inhibitors.

Journal: Chemical & pharmaceutical bulletin 20080801

Title: alpha,alpha'-disubstituted amino acids with silylated side chains as lipophilic building blocks for the synthesis of peptaibol analogues.

Journal: Chemistry & biodiversity 20080701

Title: Synthesis and ex vivo profiling of chemically modified cytomegalovirus CMVpp65 epitopes.

Journal: Journal of peptide science : an official publication of the European Peptide Society 20080301

Title: Glycine- and sarcosine-based models of vanadate-dependent haloperoxidases in sulfoxygenation reactions.

Journal: Inorganic chemistry 20070108

Title: Catalytic enantioselective synthesis of glutamic acid derivatives via tandem conjugate addition-elimination of activated allylic acetates under chiral PTC conditions.

Journal: Journal of the American Chemical Society 20051005

Title: Cinchona alkaloid-based polymer-bound phase-transfer catalysts: efficient enantioselective alkylation of benzophenone imine of glycine esters.

Journal: Molecular diversity 20050101

Title: A glycine-dependent riboswitch that uses cooperative binding to control gene expression.

Journal: Science (New York, N.Y.) 20041008

Title: Chemo-enzymatic synthesis of N-arachidonoyl glycine.

Journal: Biotechnology letters 20040801

Title: Acyclic stereoselective boron alkylation reactions for the asymmetric synthesis of beta-substituted alpha-amino acid derivatives.

Journal: Journal of the American Chemical Society 20030305

Title: The enantioselective synthesis of alpha-amino acid derivatives via organoboranes.

Journal: Journal of the American Chemical Society 20020814

Title: Chiral phosphine-free Pd-mediated asymmetric allylation of prochiral enolate with a chiral phase-transfer catalyst.

Journal: Organic letters 20011018

Title: Enantioselective synthesis of (R)-3-(3,4-dihydroxyphenyl)alanine from tert-butyl glycinate.

Journal: The Journal of organic chemistry 20010518

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SDS
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Tags:6456-74-2 Molecular Formula|6456-74-2 MDL|6456-74-2 SMILES|6456-74-2 tert-Butyl glycinate
Catalog No.: AA0038HK
6456-74-2,MFCD00038194
6456-74-2 | tert-Butyl glycinate
Pack Size： 1g
Purity： 97%
in stock
$9.00 $6.00
Pack Size： 5g
Purity： 95%
in stock
$13.00 $9.00
Pack Size： 10g
Purity： 97%
in stock
$15.00 $11.00
Pack Size： 25g
Purity： 97%
in stock
$35.00 $25.00
Pack Size： 100g
Purity： 95%
in stock
$78.00 $54.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0038HK
Chemical Name: tert-Butyl glycinate
CAS Number: 6456-74-2
Molecular Formula: C6H13NO2
Molecular Weight: 131.1729
MDL Number: MFCD00038194
SMILES: NCC(=O)OC(C)(C)C
Properties
Complexity: 104  
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: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.2  
Literature fold

Title: A powerful synergistic effect for highly efficient diastereo- and enantioselective phase-transfer catalyzed conjugate additions.

Journal: Chemical communications (Cambridge, England)20110207

Title: Synthesis and structure-activity relationships of potent 1-(2-substituted-aminoacetyl)-4-fluoro-2-cyanopyrrolidine dipeptidyl peptidase IV inhibitors.

Journal: Chemical & pharmaceutical bulletin20080801

Title: alpha,alpha'-disubstituted amino acids with silylated side chains as lipophilic building blocks for the synthesis of peptaibol analogues.

Journal: Chemistry & biodiversity20080701

Title: Synthesis and ex vivo profiling of chemically modified cytomegalovirus CMVpp65 epitopes.

Journal: Journal of peptide science : an official publication of the European Peptide Society20080301

Title: Glycine- and sarcosine-based models of vanadate-dependent haloperoxidases in sulfoxygenation reactions.

Journal: Inorganic chemistry20070108

Title: Catalytic enantioselective synthesis of glutamic acid derivatives via tandem conjugate addition-elimination of activated allylic acetates under chiral PTC conditions.

Journal: Journal of the American Chemical Society20051005

Title: Cinchona alkaloid-based polymer-bound phase-transfer catalysts: efficient enantioselective alkylation of benzophenone imine of glycine esters.

Journal: Molecular diversity20050101

Title: A glycine-dependent riboswitch that uses cooperative binding to control gene expression.

Journal: Science (New York, N.Y.)20041008

Title: Chemo-enzymatic synthesis of N-arachidonoyl glycine.

Journal: Biotechnology letters20040801

Title: Acyclic stereoselective boron alkylation reactions for the asymmetric synthesis of beta-substituted alpha-amino acid derivatives.

Journal: Journal of the American Chemical Society20030305

Title: The enantioselective synthesis of alpha-amino acid derivatives via organoboranes.

Journal: Journal of the American Chemical Society20020814

Title: Chiral phosphine-free Pd-mediated asymmetric allylation of prochiral enolate with a chiral phase-transfer catalyst.

Journal: Organic letters20011018

Title: Enantioselective synthesis of (R)-3-(3,4-dihydroxyphenyl)alanine from tert-butyl glycinate.

Journal: The Journal of organic chemistry20010518

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