Diallyl N,N-diisopropylphosphoramidite

• Catalog No.: 439606
• CAS Number: 126429-21-8
• M. F.: C12H24NO2P
• M. W.: 245.298221

SYNONYMS

• Title: 己二烯 N,N-二异丙基亚磷酰胺
• IUPAC name: [bis(prop-2-en-1-yloxy)phosphanyl]bis(propan-2-yl)amine
• IUPAC Traditional name: [bis(prop-2-en-1-yloxy)phosphanyl]diisopropylamine
• Synonyms: Diallyloxy(diisopropylamino)phosphine; N,N-Bis(1-methylethyl)phosphoramidous acid di-2-propenyl ester

DATABASE IDS

• PubChem SID: 24867522
• Beilstein Number: 4383514
• MDL Number: MFCD00216647
• CAS Number: 126429-21-8

PROPERTIES

• Linear Formula: [(CH3)2CH]2NP(OCH2CH=CH2)2
• Boiling Point: 130 °C(lit.)
• Density: 0.928 g/mL at 25 °C(lit.)
• Flash Point: 32 °C
• Flash Point: 89.6 °F
• Refractive Index: n20/D 1.456(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H226-H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
• GHS Precautionary statements: P261-P305 + P351 + P338
• RID/ADR: UN 1993 3/PG 3
• Risk Statements: 10-36/37/38
• Safety Statements: 26-36
• Storage Temperature: 2-8°C
• Hazard Class: 3
• UN Number: 1993
• Packing Group: 3
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1 g in glass bottle
Application
Precursor involved in the synthesis of pharmacologically active molecules including:
• Selective orally active S1P1 agonists1
• Water-soluble prodrugs of triazole CS-758 with antifungal activity2
• Fostriecin analogs as antitumor agents3Reactant involved in:
• Phosphitylation of alcohols4
• Deallylation for the synthesis of nucleoside phosphoramidite5
• Posphitylation and stereoselective Pudovik rearrangement6

Description (简体中文)

包装
1 g in glass bottle
Application
Precursor involved in the synthesis of pharmacologically active molecules including:
• Selective orally active S1P1 agonists1
• Water-soluble prodrugs of triazole CS-758 with antifungal activity2
• Fostriecin analogs as antitumor agents3Reactant involved in:
• Phosphitylation of alcohols4
• Deallylation for the synthesis of nucleoside phosphoramidite5
• Posphitylation and stereoselective Pudovik rearrangement6