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81477-94-3 | tert-Butyl 2-((diphenylmethylene)amino)acetate
CAS No: 81477-94-3 Catalog No: AG003SEC MDL No:MFCD00134280
Product Description
Catalog Number:
AG003SEC
Chemical Name:
tert-Butyl 2-((diphenylmethylene)amino)acetate
CAS Number:
81477-94-3
Molecular Formula:
C19H21NO2
Molecular Weight:
295.3755
MDL Number:
MFCD00134280
IUPAC Name:
tert-butyl 2-(benzhydrylideneamino)acetate
InChI:
InChI=1S/C19H21NO2/c1-19(2,3)22-17(21)14-20-18(15-10-6-4-7-11-15)16-12-8-5-9-13-16/h4-13H,14H2,1-3H3
InChI Key:
YSHDPXQDVKNPKA-UHFFFAOYSA-N
SMILES:
O=C(OC(C)(C)C)CN=C(c1ccccc1)c1ccccc1
Properties
Complexity:
363
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
295.157g/mol
Formal Charge:
0
Heavy Atom Count:
22
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
295.382g/mol
Monoisotopic Mass:
295.157g/mol
Rotatable Bond Count:
6
Topological Polar Surface Area:
38.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.4
Literature
| Title | Journal |
|---|---|
| Synthesis of main-chain chiral quaternary ammonium polymers for asymmetric catalysis using quaternization polymerization. | Molecules (Basel, Switzerland) 20120619 |
| Molecular design of chiral quaternary ammonium polymers for asymmetric catalysis applications. | Organic & biomolecular chemistry 20120414 |
| A powerful synergistic effect for highly efficient diastereo- and enantioselective phase-transfer catalyzed conjugate additions. | Chemical communications (Cambridge, England) 20110207 |
| Main-chain ionic chiral polymers: synthesis of optically active quaternary ammonium sulfonate polymers and their application in asymmetric catalysis. | Journal of the American Chemical Society 20100310 |
| Synthetic studies on (-)-lemonomycin: an efficient asymmetric synthesis of lemonomycinone amide. | The Journal of organic chemistry 20090306 |
| Combinatorial design of simplified high-performance chiral phase-transfer catalysts for practical asymmetric synthesis of alpha-alkyl- and alpha,alpha-dialkyl-alpha-amino acids. | Chemistry, an Asian journal 20080901 |
| An efficient synthesis of the constrained peptidomimetic 2-oxo-3-(N-9-fluorenyloxycarbonylamino)-1-azabicyclo[4.3.0]nonane-9-carboxylic acid from pyroglutamic acid. | The Journal of organic chemistry 20051125 |
| Cinchona alkaloid-based polymer-bound phase-transfer catalysts: efficient enantioselective alkylation of benzophenone imine of glycine esters. | Molecular diversity 20050101 |
| Lobocyclamide B from Lyngbya confervoides. Configuration and asymmetric synthesis of beta-hydroxy-alpha-amino acids by (-)-sparteine-mediated aldol addition. | Organic letters 20020530 |
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