200,000+ products from a single source!

sales@angenechem.com

Home > Other Building Blocks > 6456-74-2

6456-74-2

6456-74-2 | tert-butyl glycinate

CAS No: 6456-74-2 Catalog No: AG0038KC MDL No:MFCD00038194

Product Description

Catalog Number:
AG0038KC
Chemical Name:
tert-butyl glycinate
CAS Number:
6456-74-2
Molecular Formula:
C6H13NO2
Molecular Weight:
131.1729
MDL Number:
MFCD00038194
IUPAC Name:
tert-butyl 2-aminoacetate
InChI:
InChI=1S/C6H13NO2/c1-6(2,3)9-5(8)4-7/h4,7H2,1-3H3
InChI Key:
SJMDMGHPMLKLHQ-UHFFFAOYSA-N
SMILES:
NCC(=O)OC(C)(C)C

Properties

Complexity:
104  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
131.095g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
131.175g/mol
Monoisotopic Mass:
131.095g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
52.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.2  

Literature

Title Journal
A powerful synergistic effect for highly efficient diastereo- and enantioselective phase-transfer catalyzed conjugate additions. Chemical communications (Cambridge, England) 20110207
Synthesis and structure-activity relationships of potent 1-(2-substituted-aminoacetyl)-4-fluoro-2-cyanopyrrolidine dipeptidyl peptidase IV inhibitors. Chemical & pharmaceutical bulletin 20080801
alpha,alpha'-disubstituted amino acids with silylated side chains as lipophilic building blocks for the synthesis of peptaibol analogues. Chemistry & biodiversity 20080701
Synthesis and ex vivo profiling of chemically modified cytomegalovirus CMVpp65 epitopes. Journal of peptide science : an official publication of the European Peptide Society 20080301
Glycine- and sarcosine-based models of vanadate-dependent haloperoxidases in sulfoxygenation reactions. Inorganic chemistry 20070108
Catalytic enantioselective synthesis of glutamic acid derivatives via tandem conjugate addition-elimination of activated allylic acetates under chiral PTC conditions. Journal of the American Chemical Society 20051005
Cinchona alkaloid-based polymer-bound phase-transfer catalysts: efficient enantioselective alkylation of benzophenone imine of glycine esters. Molecular diversity 20050101
A glycine-dependent riboswitch that uses cooperative binding to control gene expression. Science (New York, N.Y.) 20041008
Chemo-enzymatic synthesis of N-arachidonoyl glycine. Biotechnology letters 20040801
Acyclic stereoselective boron alkylation reactions for the asymmetric synthesis of beta-substituted alpha-amino acid derivatives. Journal of the American Chemical Society 20030305
The enantioselective synthesis of alpha-amino acid derivatives via organoboranes. Journal of the American Chemical Society 20020814
Chiral phosphine-free Pd-mediated asymmetric allylation of prochiral enolate with a chiral phase-transfer catalyst. Organic letters 20011018
Enantioselective synthesis of (R)-3-(3,4-dihydroxyphenyl)alanine from tert-butyl glycinate. The Journal of organic chemistry 20010518

© 2019 Angene International Limited. All rights Reserved.