추천 제품
반응 적합성
reaction type: Grignard Reaction
농도
0.5 M in THF
bp
65 °C
density
0.951 g/mL at 25 °C
저장 온도
2-8°C
SMILES string
Br[Mg]CCC1OCCCO1
InChI
1S/C6H11O2.BrH.Mg/c1-2-6-7-4-3-5-8-6;;/h6H,1-5H2;1H;/q;;+1/p-1
InChI key
JYNXRXBIEHSSLR-UHFFFAOYSA-M
애플리케이션
(1,3-Dioxan-2-ylethyl)magnesium bromide can be used:
- In a Grignard addition-acylation method for the preparation of enamides.
- To prepare trisubstituted allenes by reacting with propargylic ammonium salts.
- In one of the key synthetic steps for the synthesis of febrifugine based antimalarial drugs.
법적 정보
Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
신호어
Warning
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Carc. 2 - Eye Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
보충제 위험성
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
No data available
Flash Point (°C)
No data available
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Exploration of a new type of antimalarial compounds based on febrifugine.
Journal of Medicinal Chemistry, 49(15), 4698-4706 (2006)
Oxonitriles: A Grignard Addition-Acylation Route to Enamides
Organic Letters, 8(21), 4903-4906 (2006)
Organic letters, 8(21), 4903-4906 (2006-10-06)
[reaction: see text] Sequential addition of three different Grignard reagents and pivaloyl chloride to 3-oxo-1-cyclohexene-1-carbonitrile installs four new bonds to generate a diverse array of cyclic enamides. Remarkably, formation of the C-magnesiated nitrile intermediate is followed by preferential acylation by
Copper-catalysed cross-coupling of alkyl Grignard reagents and propargylic ammonium salts: stereospecific synthesis of allenes
Chemical Communications (Cambridge, England), 54(60), 8343-8346 (2018)
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