Diethyl 3-butenylphosphonate

• Catalog No.: 640522
• CAS Number: 15916-48-0
• M. F.: C8H17O3P
• M. W.: 192.192541
• Purity: 95%

SYNONYMS

• Title: 3-丁烯基磷羧酸乙酯
• IUPAC name: diethyl (but-3-en-1-yl)phosphonate
• IUPAC Traditional name: diethyl but-3-en-1-ylphosphonate
• Synonyms: P-3-Buten-1-yl-phosphonic acid diethyl ester

DATABASE IDS

• PubChem SID: 24883099
• CAS Number: 15916-48-0
• MDL Number: MFCD06200726

PROPERTIES

• Linear Formula: CH2=CHCH2CH2PO(OCH2CH3)2
• Purity: 95%
• Boiling Point: 55 °C/0.55 mmHg(lit.)
• Density: 1.005 g/mL at 25 °C(lit.)
• Flash Point: 105 °C
• Flash Point: 221 °F
• GHS Signal Word: Danger
• GHS Hazard statements: H301
• European Hazard Symbols: Toxic (T)
• Personal Protective Equipment: Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
• GHS Precautionary statements: P301 + P310
• RID/ADR: UN 2810 6.1/PG 3
• Risk Statements: 25
• Safety Statements: 45
• Hazard Class: 6.1
• UN Number: 2810
• Packing Group: 3
• German water hazard class: 3

DETAILS

Description (简体中文)

包装
1, 10 g in glass bottle
Application
Reactant for synthesis of:
• Bicyclo[3.3.1]alkenone framework compounds by gold-catalyzed Diels-Alder reactions1
• Antiviral C-5-substituted pyrimidine acyclic nucleoside phosphonates selected as human thymidylate kinase substrates2
• Antimalarials via halogenation of di-Et butenylphosphonate3
• Bisphosphonate enynes4Reactant for:
• Remote supramolecular control of catalyst selectivity in hydroformlyation of alkenes5
• Intermolecular metal-catalyzed carbenoid cyclopropanations6
• Chemoenzymatic synthesis of phosphic derivatives of carbohydrates7

Description (English)

Packaging
1, 10 g in glass bottle
Application
Reactant for synthesis of:
• Bicyclo[3.3.1]alkenone framework compounds by gold-catalyzed Diels-Alder reactions1
• Antiviral C-5-substituted pyrimidine acyclic nucleoside phosphonates selected as human thymidylate kinase substrates2
• Antimalarials via halogenation of di-Et butenylphosphonate3
• Bisphosphonate enynes4Reactant for:
• Remote supramolecular control of catalyst selectivity in hydroformlyation of alkenes5
• Intermolecular metal-catalyzed carbenoid cyclopropanations6
• Chemoenzymatic synthesis of phosphic derivatives of carbohydrates7