349852

[3-(Ethoxycarbonyl)propyl]triphenylphosphonium bromide

97%

• Synonym(s): NSC 269919
• Linear Formula: C₂H₅O₂C(CH₂)₃P(C₆H₅)₃Br
• CAS Number: 50479-11-3
• Molecular Weight: 457.34
• MDL number: MFCD00274610
• UNSPSC Code: 12352108
• PubChem Substance ID: 24861713
• NACRES: NA.22

Properties

• Quality Level: 100
• Assay: 97%
• reaction suitability: reaction type: C-C Bond Formation
• mp: 165-167 °C (lit.)
• SMILES string: [Br-].CCOC(=O)CCC[P+](c1ccccc1)(c2ccccc2)c3ccccc3
• InChI: 1S/C24H26O2P.BrH/c1-2-26-24(25)19-12-20-27(21-13-6-3-7-14-21,22-15-8-4-9-16-22)23-17-10-5-11-18-23;/h3-11,13-18H,2,12,19-20H2,1H3;1H/q+1;/p-1
• InChI key: JPZMNVPVVYVXAD-UHFFFAOYSA-M

Description

Application

Reactant for:

• Asymmetric synthesis of antihypercholesterolemic ezetimibe via Wittig reaction
• Wittig reactions

[3-(Ethoxycarbonyl)propyl]triphenylphosphonium bromide can be used:

• As a reactant in the synthesis of spirocyclic GPR119 agonists.
• In the synthesis of cyclic acetal intermediate of azadirachtin, a terpenoid found in the neem tree Azadirachta indica.
• To prepare a catechin metabolite named 5-(3,4,5-trihydroxyphenyl)valeric acid.

Safety Information

• Pictograms: GHS07
• Signal Word: Warning
• Hazard Statements: H315,H319,H335
• Precautionary Statements: P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
• Hazard Classifications: Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
• Target Organs: Respiratory system
• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 3
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves