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Home Other Building Blocks 2-(Di-tert-butylphosphino)biphenyl

2-(Di-tert-butylphosphino)biphenyl

CAS No.:
224311-51-7
Catalog Number:
AG0032VJ
Molecular Formula:
C20H27P
Molecular Weight:
298.4021
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$32
- +
5g
≥98%
In Stock USA
United States
$82
- +
10g
≥98%
In Stock USA
United States
$130
- +
25g
98%
In Stock USA
United States
$300
- +
100g
98%
In Stock USA
United States
$1050
- +
Product Description
Catalog Number:
AG0032VJ
Chemical Name:
2-(Di-tert-butylphosphino)biphenyl
CAS Number:
224311-51-7
Molecular Formula:
C20H27P
Molecular Weight:
298.4021
MDL Number:
MFCD01862440
IUPAC Name:
ditert-butyl-(2-phenylphenyl)phosphane
InChI:
InChI=1S/C20H27P/c1-19(2,3)21(20(4,5)6)18-15-11-10-14-17(18)16-12-8-7-9-13-16/h7-15H,1-6H3
InChI Key:
CNXMDTWQWLGCPE-UHFFFAOYSA-N
SMILES:
CC(P(C(C)(C)C)c1ccccc1c1ccccc1)(C)C
UNII:
5Y743P380H
Properties
Complexity:
300  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
298.185g/mol
Formal Charge:
0
Heavy Atom Count:
21  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
298.41g/mol
Monoisotopic Mass:
298.185g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
5.1  
Literature
Title Journal
Influence of biaryl phosphine structure on C-N and C-C bond formation. Journal of the American Chemical Society 20090902
FeCl3-catalyzed 1,2-addition reactions of aryl aldehydes with arylboronic acids. Organic letters 20090115
Addition of alkynes to aldehydes and activated ketones catalyzed by rhodium-phosphine complexes. The Journal of organic chemistry 20071207
Synthesis of gerfelin and related analogous compounds. Bioscience, biotechnology, and biochemistry 20061001
Rhodium-catalyzed addition of alkynes to activated ketones and aldehydes. Organic letters 20060105
Stereoselective palladium-catalyzed O-glycosylation using glycals. Journal of the American Chemical Society 20040211
Synthesis of substituted oxindoles from alpha-chloroacetanilides via palladium-catalyzed C[bond]H functionalization. Journal of the American Chemical Society 20031008
A mild and efficient method for the stereoselective formation of C-O bonds: palladium-catalyzed allylic etherification using zinc(II) alkoxides. Organic letters 20021128
Improved synthesis of aryltriethoxysilanes via palladium(0)-catalyzed silylation of aryl iodides and bromides with triethoxysilane. The Journal of organic chemistry 20011102
Properties