V1902
Vinyl bromide
98%
Synonyme(s) :
Bromoethylene
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About This Item
Formule linéaire :
CH2=CHBr
Numéro CAS:
Poids moléculaire :
106.95
Beilstein:
1361370
Numéro CE :
Numéro MDL:
Code UNSPSC :
12162002
ID de substance PubChem :
Nomenclature NACRES :
NA.23
Produits recommandés
Densité de vapeur
3.8 (15 °C, vs air)
Niveau de qualité
Pression de vapeur
1551 mmHg ( 37.8 °C)
Essai
98%
Température d'inflammation spontanée
986 °F
Contient
200 ppm monomethyl ether hydroquinone as inhibitor
Limite d'explosivité
15 %
pb
16 °C/750 mmHg (lit.)
Pf
−139 °C (lit.)
Densité
1.517 g/mL at 25 °C (lit.)
Température de stockage
2-8°C
Chaîne SMILES
BrC=C
InChI
1S/C2H3Br/c1-2-3/h2H,1H2
Clé InChI
INLLPKCGLOXCIV-UHFFFAOYSA-N
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Catégories apparentées
Application
- 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).
Autres remarques
V1902-100 g, V1902-900 g, and 1902-2.2 kg includes installed 316SS needle valve.
Produits recommandés
Stainless steel hose adapter Z146838 or stainless steel body mini gas regulator Z513547 is recommended.
Raccord cannelé
Réf. du produit
Description
Tarif
Régulateur
Réf. du produit
Description
Tarif
Mention d'avertissement
Danger
Mentions de danger
Conseils de prudence
Classification des risques
Acute Tox. 4 Oral - Carc. 1B - Flam. Gas 1A - Press. Gas Liquefied gas
Code de la classe de stockage
2A - Gases
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
55.4 °F
Point d'éclair (°C)
13 °C
Équipement de protection individuelle
Eyeshields, Faceshields, Gloves
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Les clients ont également consulté
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
Qiwu Zhao et al.
Organic letters, 10(18), 4037-4040 (2008-08-30)
A general and highly efficient synthesis of 4-alkylidene-2-azetidinones was achieved by the Cu(I)-catalyzed intramolecular C-N coupling of amides with vinyl bromides. This 4-exo ring closure was found to be fundamentally preferred over other modes (5-exo, 6-exo, and 6-endo) of cyclization
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
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