V1902
Vinyl bromide
98%
Sinónimos:
Bromoethylene
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About This Item
Fórmula lineal:
CH2=CHBr
Número de CAS:
Peso molecular:
106.95
Beilstein:
1361370
Número CE:
Número MDL:
Código UNSPSC:
12162002
ID de la sustancia en PubChem:
NACRES:
NA.23
Productos recomendados
densidad de vapor
3.8 (15 °C, vs air)
Nivel de calidad
presión de vapor
1551 mmHg ( 37.8 °C)
Ensayo
98%
temp. de autoignición
986 °F
contiene
200 ppm monomethyl ether hydroquinone as inhibitor
lim. expl.
15 %
bp
16 °C/750 mmHg (lit.)
mp
−139 °C (lit.)
densidad
1.517 g/mL at 25 °C (lit.)
temp. de almacenamiento
2-8°C
cadena SMILES
BrC=C
InChI
1S/C2H3Br/c1-2-3/h2H,1H2
Clave InChI
INLLPKCGLOXCIV-UHFFFAOYSA-N
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Categorías relacionadas
Aplicación
- FTIR and Raman Spectroscopy Study of Soot Deposits: Investigates soot formation during the infrared multiphoton dissociation of vinyl bromide, suggesting potential applications in materials science regarding soot characteristics (Samoudi et al., 2022).
- Nickel-Catalyzed Reductive Cross-Coupling: Describes a method for coupling vinyl bromides with unactivated alkyl halides, highlighting its utility in synthetic organic chemistry for creating complex molecules (Gong et al., 2017).
- Silver-Promoted Synthesis of Vinyl Sulfones: This study explores the reactivity of vinyl bromides with sulfonyl hydrazides under aqueous conditions, applicable to pharmaceutical synthesis due to the biorelevance of sulfones (Zhang et al., 2020).
- Visible Light on Vinyl Halides: Examines the photocatalytic properties of vinyl bromides, which could influence the development of green chemistry applications (Pagire et al., 2020).
- Palladium Catalyzed Cross-Coupling of Diboronates: Focuses on the reactions of vinyl bromides with diboronates, offering insights into new methodologies for constructing biologically active compounds (Li et al., 2014).
Otras notas
V1902-100 g, V1902-900 g, and 1902-2.2 kg includes installed 316SS needle valve.
Productos recomendados
Stainless steel hose adapter Z146838 or stainless steel body mini gas regulator Z513547 is recommended.
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Referencia del producto
Descripción
Precios
regulador
Referencia del producto
Descripción
Precios
Palabra de señalización
Danger
Frases de peligro
Consejos de prudencia
Clasificaciones de peligro
Acute Tox. 4 Oral - Carc. 1B - Flam. Gas 1A - Press. Gas Liquefied gas
Código de clase de almacenamiento
2A - Gases
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
55.4 °F
Punto de inflamabilidad (°C)
13 °C
Equipo de protección personal
Eyeshields, Faceshields, Gloves
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Los clientes también vieron
Carcinogenicity of 1,3-butadiene, ethylene oxide, vinyl chloride, vinyl fluoride, and vinyl bromide.
Yann Grosse et al.
The Lancet. Oncology, 8(8), 679-680 (2007-08-30)
Piotr Pawluć et al.
Organic letters, 11(15), 3390-3393 (2009-07-04)
A new, efficient protocol for the highly stereoselective one-pot synthesis of (E)-beta-aryl vinyl iodides and (E)-beta-aryl vinyl bromides from styrenes based on sequential ruthenium-catalyzed silylative coupling-N-halosuccinimide-mediated halodesilylation reactions is reported.
Cheon-Gyu Cho et al.
Organic letters, 7(16), 3569-3572 (2005-07-29)
An effective, readily scalable two-step synthesis of trisubstituted (E)-vinyl bromides involving bromination of alpha,beta-unsaturated lactones followed by hydrolytic fragmentation has been developed. Several trisubstituted (E)-vinyl bromides, including multigram quantities of (+)-(E)-4-bromo-2-methyl-3-pentenol, a synthetic intermediate required for the C(8)-C(11) moieties of
Hsin-Lun Kao et al.
Organic letters, 13(19), 5204-5207 (2011-09-02)
The synthesis of vinyl sulfides through the coupling reaction of thiols with vinyl iodides, bromides, and chlorides is described. The thiols can couple with aryl iodides in the presence of only 0.5 mol % Cu(2)O without the need for an
Changhui Sun et al.
Organic letters, 11(18), 4084-4087 (2009-08-20)
With the catalysis of CuI/trans-N,N'-dimethylcyclohexane-1,2-diamine, a number of carboxylic acids underwent efficient intramolecular O-vinylation with vinyl bromides leading to the synthesis of the corresponding five- and six-membered enol lactones. The same catalytic system also led to the efficient cycloisomerization of
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