V1902
Vinyl bromide
98%
Synonim(y):
Bromoethylene
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About This Item
Wzór liniowy:
CH2=CHBr
Numer CAS:
Masa cząsteczkowa:
106.95
Beilstein:
1361370
Numer WE:
Numer MDL:
Kod UNSPSC:
12162002
Identyfikator substancji w PubChem:
NACRES:
NA.23
Polecane produkty
gęstość pary
3.8 (15 °C, vs air)
Poziom jakości
ciśnienie pary
1551 mmHg ( 37.8 °C)
Próba
98%
temp. samozapłonu
986 °F
zawiera
200 ppm monomethyl ether hydroquinone as inhibitor
granice wybuchowości
15 %
tw
16 °C/750 mmHg (lit.)
mp
−139 °C (lit.)
gęstość
1.517 g/mL at 25 °C (lit.)
temp. przechowywania
2-8°C
ciąg SMILES
BrC=C
InChI
1S/C2H3Br/c1-2-3/h2H,1H2
Klucz InChI
INLLPKCGLOXCIV-UHFFFAOYSA-N
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Powiązane kategorie
Zastosowanie
- 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).
Inne uwagi
V1902-100 g, V1902-900 g, and 1902-2.2 kg includes installed 316SS needle valve.
Polecane produkty
Stainless steel hose adapter Z146838 or stainless steel body mini gas regulator Z513547 is recommended.
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króciec do węża
Numer produktu
Opis
Cennik
regulator
Numer produktu
Opis
Cennik
Hasło ostrzegawcze
Danger
Zwroty wskazujące rodzaj zagrożenia
Zwroty wskazujące środki ostrożności
Klasyfikacja zagrożeń
Acute Tox. 4 Oral - Carc. 1B - Flam. Gas 1A - Press. Gas Liquefied gas
Kod klasy składowania
2A - Gases
Klasa zagrożenia wodnego (WGK)
WGK 3
Temperatura zapłonu (°F)
55.4 °F
Temperatura zapłonu (°C)
13 °C
Środki ochrony indywidualnej
Eyeshields, Faceshields, Gloves
Certyfikaty analizy (CoA)
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
Klienci oglądali również te produkty
James A Marshall et al.
Organic letters, 6(3), 445-448 (2004-01-30)
[reaction: see text] Additions of vinylic zinc bromide reagents to alpha-chiral aldehydes (R(1) = CH(2)OTBS, R(2) = Me; R(1) = Me, R(2) = OTBS) in the presence of lithiated (+)- or (-)-N-methylephedrine proceed with predominant reagent control to afford anti
Qiwu Zhao et al.
The Journal of organic chemistry, 74(1), 459-462 (2008-11-27)
With CuI as the catalyst and K(3)PO(4) x 3 H(2)O as the base, highly efficient intramolecular S-vinylation of thiols with vinyl chlorides or bromides was successfully implemented without the help of an additional ligand. Moreover, the competition experiments revealed that
Bryden A F Le Bailly et al.
Chemical communications (Cambridge, England), 48(10), 1580-1582 (2011-11-02)
An iron-catalysed, hydride-mediated reductive cross-coupling reaction has been developed for the preparation of alkanes. Using a bench-stable iron(II) pre-catalyst, reductive cross-coupling of vinyl iodides, bromides and chlorides with aryl- and alkyl Grignard reagents successfully gave the products of formal sp(3)-sp(3)
Mina Lee et al.
The Journal of chemical physics, 123(17), 174310-174310 (2005-12-27)
The vibrational spectrum of the vinyl bromide cation in the first excited electronic state A 2A' was obtained by one-photon mass-analyzed threshold ionization (MATI) spectroscopy. The use of an improved vacuum-ultraviolet radiation source based on four-wave sum frequency mixing in
Xiaodan Zhao et al.
The Journal of organic chemistry, 71(10), 3988-3990 (2006-05-06)
(E/Z)-isomers containing vinyl bromides were stereoselectively carbonylated to the corresponding (E)-alpha,beta-ethylenic carboxylic acids in the ionic liquid [BMIM]PF6. Vinyl dibromides also underwent hydroxycarbonylation to give monoacids. The products are pure by proton NMR spectroscopic determination without purification by silica gel
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