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39319-11-4 molecular structure
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ChemBase ID: 141974
Molecular Formular: C18H14P
Molecular Mass: 261.277521
Monoisotopic Mass: 261.08331208
SMILES and InChIs

SMILES:
*c1ccc(cc1)P(c1ccccc1)c1ccccc1
Canonical SMILES:
*c1ccc(cc1)P(c1ccccc1)c1ccccc1
InChI:
InChI=
InChIKey:

Cite this record

CBID:141974 http://www.chembase.cn/molecule-141974.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
Synonyms
JandaJel™-triphenylphosphine
Copolymer of styrene and divinylbenzene, diphenylphosphinated
Diphenylphosphino-polystyrene
Polystyrene crosslinked with divinylbenzene, diphenylphosphinated
Triphenylphosphine, polymer-bound
Triphenylphosphine, polymer-supported, 1.4-2.0 mmol/g on polystyrene
JandaJel™-三苯基膦
二苯基膦-聚苯乙烯
聚苯乙烯交联二乙烯基苯,二苯基磷化
苯乙烯-二乙烯基苯共聚物,二苯基磷化
聚合物键合型三苯基膦
三苯基膦, 聚合物负载, 1.4-2.0 mmol/g于聚苯乙烯
CAS Number
39319-11-4
MDL Number
MFCD00148025
MFCD03703012
PubChem SID
24862656
24889790
24877960
24889791
162236206
24848790
PubChem CID
11776

CALCULATED PROPERTIES

CALCULATED PROPERTIES

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
European Hazard Symbols
X expand Show data source
Irritant Irritant (Xi) expand Show data source
Harmful Harmful (Xn) expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
20/21/22-36/37/38 expand Show data source
22-43-53 expand Show data source
36/37/38 expand Show data source
Safety Statements
24-37-60-61 expand Show data source
26-36 expand Show data source
TSCA Listed
expand Show data source
GHS Pictograms
GHS06 expand Show data source
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H301-H317-H413 expand Show data source
H302-H312-H315-H319-H332-H335 expand Show data source
H315-H319-H335 expand Show data source
GHS Precautionary statements
P261-P280-P305 + P351 + P338 expand Show data source
P261-P301+P310-P302+P352-P321-P405-P501A expand Show data source
P261-P305 + P351 + P338 expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Faceshields, Gloves expand Show data source
dust mask type N95 (US), Eyeshields, Gloves expand Show data source
Storage Temperature
2-8°C expand Show data source
Particle Size
100-200 mesh expand Show data source
200-400 mesh expand Show data source
50-100 mesh expand Show data source
Extent of Labeling
~1.6 mmol/g loading expand Show data source
~3 mmol/g triphenylphosphine loading expand Show data source
~3.0 mmol/g loading expand Show data source
~3.0 mmol/g P loading expand Show data source
~3.2 mmol/g loading expand Show data source
Matrix
crosslinked with 1% DVB expand Show data source
crosslinked with 2% DVB expand Show data source
Crosslinking
2 % cross-linked expand Show data source
2 % cross-linked with divinylbenzene expand Show data source
Linear Formula
-C6H4P(C6H5)2 expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 93094 external link
Packaging
5, 25 g in glass bottle
Sigma Aldrich - 366455 external link
Packaging
5, 25, 100 g in glass bottle
Preparation Note
Used for the preparation of supported precious metal complexes.1
Used to prepare polymer bound ylides for Wittig reactions. It can also be used to convert alcohols or carboxylic acids to the corresponding chlorides under relatively mild conditions in high yield.
Sigma Aldrich - 533416 external link
Packaging
5 g in glass bottle
Legal Information
JandaJel is a trademark of Sigma-Aldrich Co. LLC
Sigma Aldrich - 93093 external link
Other Notes
Polymer-bound triphenylphosphine is used for preparing polymer-bound yields which are highly useful for Wittig reactions; removal of the polymer at the end of the reaction removes all the phosphine oxide.1,2
Packaging
5, 25 g in glass bottle
Sigma Aldrich - 14664 external link
Packaging
5, 25 g in poly bottle

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Support for nickel, rhenium and rhodium in hydrogenation: J. Am. Chem. Soc., 97, 1742 (1975); dimerization of alkenes: J. Am. Chem. Soc., 97, 341 (1974) and hydroformylation: J. Am. Chem. Soc., 98 5402 (1976). For the halogenation of carboxylic acid and alkanes in carbon tetrachloride: Synthesis, 1093 (1992). Addition of iodine in DMF esterifies primary and secondary alcohols to their respective formate esters: Med. Res. Rev., 19, 97 (1999).
  • • For use in the Mitsunobu reaction: Tetrahedron Lett., 8751 (1998), and the Wittig reaction: J. Org. Chem., 48, 326 (1983); J. Chem. Soc. Perkin 1, 2243 (1998).
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PATENTS

PATENTS

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INTERNET

INTERNET

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