추천 제품
Quality Level
분석
95%
refractive index
n20/D 1.495 (lit.)
bp
195 °C (lit.)
density
1.013 g/mL at 25 °C (lit.)
작용기
ether
SMILES string
C1CC2OC2CCC=C1
InChI
1S/C8H12O/c1-2-4-6-8-7(9-8)5-3-1/h1-2,7-8H,3-6H2/b2-1-
InChI key
YWFPXWMSGJXUFS-UPHRSURJSA-N
일반 설명
9-Oxabicyclo[6.1.0]non-4-ene is an epoxide. It undergoes halofluorination reactions with N-halosuccinimides and triethylamine tris-hydrofluoride or Olah′s reagent.
애플리케이션
9-Oxabicyclo[6.1.0]non-4-ene may be used in the following studies:
- novel bicyclo[4.2.1] and bicyclo[3.3.1] ethers
- trans, trans-2,6-dibromo-9-oxabicyclo[3.3.1]nonane and trans, trans-2,5-dibromo-9-oxabicyclo[4.2.1]nonane
- (Z)-2-(cyclooct-4-enyloxy)acetic acid.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
158.0 °F - closed cup
Flash Point (°C)
70 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
High-yielding, two-step 18F labeling strategy for 18F-PARP1 inhibitors.
ChemMedChem, 6(3), 424-427 (2011-03-02)
Stereoselective synthesis of cyclic ethers via bromine assistedepoxide ring expansion.
Tetrahedron Letters, 26(11), 1461-1464 (1985)
The Journal of organic chemistry, 76(1), 97-104 (2010-12-01)
9-Oxabicyclo[6.1.0]non-4-ene (1) undergoes intramolecular bromonium ion-assisted epoxide ring-opening using N-bromosuccinimide via a presumed oxonium ion that is subject to stereospecific, nonregioselective capture with added external nucleophiles producing novel bicyclo[4.2.1] and bicyclo[3.3.1] ethers. Carboxylic acids (as catalyzed by tetramethylguanidine), alcohols, water
Transannular oxygen participation in halofluorination reactions of 9-oxabicyclo [6.1. 0] non-4-ene [1].
Journal of Fluorine Chemistry, 46(1), 83-95 (1990)
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