|
| (4-Carboxybutyl)triphenylphosphonium bromide Basic information |
| (4-Carboxybutyl)triphenylphosphonium bromide Chemical Properties |
Melting point | 204-207 °C(lit.) | Boiling point | 324.7-327.4℃ at 101.93-102.15kPa | density | 1.371 at 20℃ | vapor pressure | 0Pa at 25℃ | Fp | 195°(383°F) | storage temp. | Store below +30°C. | solubility | DMSO, Methanol, Water | form | solid | color | White to Off-White | Water Solubility | Soluble in ethanol, methanol and soluble water. Insoluble in toluene and hexane. | Sensitive | Hygroscopic | BRN | 3586477 | InChIKey | KQJPHSBFOSLICV-UHFFFAOYSA-N | LogP | 0.146 | CAS DataBase Reference | 17814-85-6(CAS DataBase Reference) |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26-36 | RIDADR | 3278 | WGK Germany | 3 | HS Code | 29310095 |
| (4-Carboxybutyl)triphenylphosphonium bromide Usage And Synthesis |
Chemical Properties | WHITE TO ALMOST WHITE CRYSTALLINE POWDER | Uses | - Used as a platform for delivery of pro-apoptotic peptides into the mitochondria of tumor cells
Reactant for preparation of:
- Ring skeletons via ring closing metathesis and double bond migration ring closing metathesis reactions
- Methyl alkenyl quinolones as antimycobacterial agents
- Prostaglandins and their drug analogs via Gold-catalyzed Meyer-Schuster rearrangement
- Diphenylmethylpiperazines as N-type calcium channel blockers as potential therapeutic agents
- Folate receptor-specific glycinamide ribonucleotide formyltransferase (GARFTase) inhibitors with antitumor activity
- Cycloalkylidene alkanols with antileishmanial activity, via Wittig reaction
| Uses | suzuki reaction | Uses | (4-Carboxybutyl)triphenylphosphonium Bromide (cas# 17814-85-6) is a compound useful in organic synthesis. |
| (4-Carboxybutyl)triphenylphosphonium bromide Preparation Products And Raw materials |
|