1,1′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenylphosphine]
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1,1′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenylphosphine]
structure -
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CAS No:
161265-03-8
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Formula:
C39H32OP2
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Chemical Name:
1,1′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenylphosphine]
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Synonyms:
Phosphine,1,1′-(9,9-dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenyl-;Phosphine,(9,9-dimethyl-9H-xanthene-4,5-diyl)bis[diphenyl-;1,1′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenylphosphine];Xantphos;(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis[diphenylphosphine];4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene;9,9-Dimethyl-4,5-bis(diphenylphosphino)xanthene;4,5-Bis(diphenylphosphino)-9,9-dimethyl-9H-xanthene;9,9-Dimethyl-4,5-bis(diphenylphosphino)-9H-xanthene;(9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphane);(5-Diphenylphosphanyl-9,9-dimethylxanthen-4-yl)-diphenylphosphane;(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine)
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CAS No:
1,1′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenylphosphine] Basic Attributes
578.62
578.62
1308068-626-2
NMU72MOG9B
DTXSID20348350
2932999099
Characteristics
9.2
9.7
White to light yellow Crystals
229-230 °C
665.7°C at 760 mmHg
450℃
soluble in organic solvents.
Room temperature.
7.61E-17mmHg at 25°C
Safety Information
3
37-20/22
37/39-26
Xn
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
H315
|Warning|H315 (75.54%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 141 companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
1,1′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenylphosphine] Use and Manufacturing
As a ligand, it is used in coupling reactions such as Buchwald and Suzuki; organic reagents and pharmaceutical intermediates. 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene; metal complexes can be used as organic synthesis catalysts such as carbonylation reactions; in the cross-coupling of 3-bromothiophene and 2-aminopyridine CN catalyzed by palladium Ligand in ring synthesis reaction; also used in ruthenium-catalyzed activation of the alkylation reaction of methylene compounds with ethanol; metal chelate ligand used in catalysis
Computed Properties
Molecular Weight:578.6
XLogP3:9.7
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:6
Exact Mass:578.19283964
Monoisotopic Mass:578.19283964
Topological Polar Surface Area:9.2
Heavy Atom Count:42
Complexity:731
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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1,1′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenylphosphine]
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