추천 제품
vapor density
4.2 (vs air)
Quality Level
제품 라인
ReagentPlus®
분석
99%
형태
liquid
autoignition temp.
554 °F
포함
≤1000 ppm propylene oxide as stabilizer
expl. lim.
7.3 %
refractive index
n20/D 1.469 (lit.)
bp
70-71 °C (lit.)
mp
−119 °C (lit.)
density
1.398 g/mL at 25 °C (lit.)
저장 온도
2-8°C
SMILES string
BrCC=C
InChI
1S/C3H5Br/c1-2-3-4/h2H,1,3H2
InChI key
BHELZAPQIKSEDF-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Allyl bromide can be used as a reagent to prepare:
- Allyl ketones by Barbier-type allylation of various nitriles in the presence of Lewis acid.
- Homoallylic alcohols by reacting with aldehydes or ketones using zinc dust as a catalyst.
- 1,5-hexadiene by reductive C-C bond coupling using silver hydride cluster.
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Carc. 1B - Eye Dam. 1 - Flam. Liq. 2 - Muta. 1B - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
30.2 °F - closed cup
Flash Point (°C)
-1 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Facile and efficient synthesis of homoallylic alcohols using allyl bromide and commercial zinc dust
Tetrahedron Letters, 36(27), 4885-4888 (1995)
Gas-phase synthesis of [Ag4H]+ and its mediation of the C-C coupling of allyl bromide
Angewandte Chemie (International Edition in English), 44(5), 728-731 (2005)
Synthesis of allyl ketone via Lewis acid promoted Barbier-type reaction
Tetrahedron Letters, 41(45), 8803-8806 (2000)
Materials (Basel, Switzerland), 13(11) (2020-06-11)
The superior ability of thiiranes (episulfides) to undergo ring-opening polymerization (ROP) in the presence of anionic initiators allows the preparation of chemically stable polysulfide homopolymers. Incorporation of elemental sulfur (S8) by copolymerization below the floor temperature of S8 permits the
Chemical communications (Cambridge, England), (40)(40), 4209-4211 (2006-10-13)
The total synthesis of natural (4R,5R)-antillatoxin and its analog (4S,5S)-antillatoxin has been achieved; the optically pure key intermediates were prepared from indium mediated allylation of either primary or secondary allylic bromide with aldehyde in aquoues media, followed by highly selective
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