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ChemicalBook--->CAS DataBase List--->18355-96-9

18355-96-9

18355-96-9 Structure

18355-96-9 Structure
IdentificationBack Directory
[Name]

3-((Dimethylamino)propyl)triphenylphosphonium bromide
[CAS]

18355-96-9
[Synonyms]

Olopatadine int
(3-(Dimethylamino)
Olopatadine Impurity 19
3-(dimethylamino)propyl-triphenylphosphanium
(3-Dimethylamino)propyltriphenylphosphonium bromide
(3-BROMIDEPROPYL)TRIPHENYLPHOS-PHONIUM BROMIDE, 98+%
(3-(Dimethylamino)propyl)triphenylphosphonium bromide 98%
(3-(DiMethylaMino)propyl)triphenylphosphoniuM broMide
3-(DIMETHYLAMINO)PROPYL]TRIPHENYLPHOSPHONIUM BROMIDE [WITTING REAGENT
(3-(DiMethylaMino)propyl)triphenylphosphoniuM broMide(3-(DiMethylaMino)propyl)triphenylphosphoniuM broMide
[EINECS(EC#)]

605-998-7
[Molecular Formula]

C23H27BrNP
[MDL Number]

MFCD00012200
[MOL File]

18355-96-9.mol
[Molecular Weight]

428.35
Chemical PropertiesBack Directory
[Melting point ]

193-196 °C
[storage temp. ]

Inert atmosphere,Room Temperature
[BRN ]

4637548
[InChIKey]

SSWPSKSQQSJKKF-UHFFFAOYSA-M
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

(3-(Dimethylamino)propyl)triphenyl-phosphonium Bromide is used in preparation of olopatadine hydrochloride.
[Uses]

Reactant for preparation of:
  • Topoisomerase I-targeting antitumor agents
  • C15-C21 stereopentad of discodermolide via cleavage of aminoglycosides, double-bond isomerization, and selective hydroxyl group protection
  • Diphenyl amine based sodium channel blockers, effective against hNav1.2

  • Reactant for Wittig reaction with benzaldehyde
[reaction suitability]

reaction type: C-C Bond Formation
Spectrum DetailBack Directory
[Spectrum Detail]

3-((Dimethylamino)propyl)triphenylphosphonium bromide(18355-96-9)1HNMR
3-((Dimethylamino)propyl)triphenylphosphonium bromide(18355-96-9)FT-IR
3-((Dimethylamino)propyl)triphenylphosphonium bromide(18355-96-9)Raman
3-((Dimethylamino)propyl)triphenylphosphonium bromide(18355-96-9)IR
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