(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide NEW

$15.00 100kg

$18.00 10kg

$20.00 1kg

Hebei Duling International Trade Co. LTD

3YR

China

Chemical Properties

Product Name	(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide
CAS No	52509-14-5
EC-No	257-977-3
Min. Order	1kg
Purity	99%
Supply Ability	5000 tons
Release date	2024/05/27

(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide Basic information

Product Name:	(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide
Synonyms:	LABOTEST-BB LT00233112;(1,3-DIOXOLAN-2-YLMETHYL)TRIPHENYLPHOSPHONIUM BROMIDE;(1,3-DIOXOLANE-2-YL METHYL) TRIPHENYL PHOSPHONIUM BROMIDE;TRIPHENYL-1,3-DIOXOLAN-2-YLMETHYL-PHOSPHONIUM BROMIDE;2-(1,3)-DIOXOLANE-2-YL-METHYLTRIPHENYLPHOSPHONIUM BROMIDE;(1,3-DIOXOLAN-2-YLMETHYL)TRIPHENYLPHOSPHONIUM BROMIDE 98%;(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide, 98 %;Phosphonium, (1,3-dioxolan-2-ylmethyl)triphenyl-, bromide
CAS:	52509-14-5
MF:	C22H22BrO2P
MW:	429.29
EINECS:	257-977-3
Product Categories:	Dioxanes & Dioxolanes;Dioxolanes;Phosphonium Compounds;Synthetic Organic Chemistry;Wittig & Horner-Emmons Reaction;Wittig Reaction;C-C Bond Formation;Olefination;Wittig Reagents
Mol File:	52509-14-5.mol

(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide Chemical Properties

Melting point	193-195 °C(lit.)
storage temp.	Store below +30°C.
solubility	Chloroform (Slightly), Methanol (Slightly)
form	Powder or Crystals
color	White to light brown
Water Solubility	Soluble in water (20°C).
Sensitive	Hygroscopic
InChIKey	FRHRVQQUICVJDG-UHFFFAOYSA-M
CAS DataBase Reference	52509-14-5(CAS DataBase Reference)

Safety Information

MSDS Information

Provider	Language
(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide	English
SigmaAldrich	English
ACROS	English

(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide Usage And Synthesis

Chemical Properties	white to light brown granular powder
Uses	(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium Bromide is used as a reactant in the synthesis of ketolides methyloxoerythromycins with antibacterial activity as highly potent against macrolide-resistant and susceptible respiratory pathogens.
Uses	Reactant for: Preparation of a ratiometric fluorescent probe for specific detection of cysteine over homocysteine and glutathione Microwave-assisted synthesis of KN-93 as inhibitor of calmodulin kinase II Preparation of fluorinated spirobenzofuran piperidines as s1 receptor ligands Synthesis and antitumor agents Regio-selective preparation of indole derivatives via rhodium-catalyzed domino hydroformylation/indolization
Purification Methods	Wash the crystals with Et2O, dry them in a vacuum and recrystallise them from CH2Cl2/dry Et2O to give prisms m 172-174o, which is raised to 191.5-193o on drying at 56o/0.5mm. [Cresp et al. J Chem Soc, Perkin Trans 1 37 1974.]

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