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Home Other Building Blocks Ethyl (triphenylphosphoranylidene) acetate

Ethyl (triphenylphosphoranylidene) acetate

CAS No.:
1099-45-2
Catalog Number:
AG0034TU
Molecular Formula:
C22H21O2P
Molecular Weight:
348.3747
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
25g
97%
In Stock USA
United States
$25
- +
100g
97%
In Stock USA
United States
$63
- +
500g
97%
In Stock USA
United States
$225
- +
Product Description
Catalog Number:
AG0034TU
Chemical Name:
Ethyl (triphenylphosphoranylidene) acetate
CAS Number:
1099-45-2
Molecular Formula:
C22H21O2P
Molecular Weight:
348.3747
MDL Number:
MFCD00009183
IUPAC Name:
ethyl 2-(triphenyl-λ5-phosphanylidene)acetate
InChI:
InChI=1S/C22H21O2P/c1-2-24-22(23)18-25(19-12-6-3-7-13-19,20-14-8-4-9-15-20)21-16-10-5-11-17-21/h3-18H,2H2,1H3
InChI Key:
IIHPVYJPDKJYOU-UHFFFAOYSA-N
SMILES:
CCOC(=O)C=P(c1ccccc1)(c1ccccc1)c1ccccc1
EC Number:
214-151-7
NSC Number:
72406
Properties
Complexity:
414  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
348.128g/mol
Formal Charge:
0
Heavy Atom Count:
25  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
348.382g/mol
Monoisotopic Mass:
348.128g/mol
Rotatable Bond Count:
6  
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.3  
Literature
Title Journal
The synthesis of a new class of chiral pincer ligands and their applications in enantioselective catalytic fluorinations and the Nozaki-Hiyama-Kishi reaction. Chemistry (Weinheim an der Bergstrasse, Germany) 20111223
Enantioselective organocatalytic Michael-Wittig-Michael-Michael reaction: dichotomous construction of pentasubstituted cyclopentanecarbaldehydes and pentasubstituted cyclohexanecarbaldehydes. Organic letters 20110318
A facile one-pot synthesis of alpha-bromo-alpha,beta-unsaturated esters from alcohols. Molecules (Basel, Switzerland) 20100504
Ethyl 3-[2-(p-toluene-sulfonamido)phen-yl]acrylate. Acta crystallographica. Section E, Structure reports online 20091001
Potent new small-molecule inhibitor of botulinum neurotoxin serotype A endopeptidase developed by synthesis-based computer-aided molecular design. PloS one 20090101
An efficient synthesis of tetramic acid derivatives with extended conjugation from L-ascorbic acid. Beilstein journal of organic chemistry 20060101
Properties