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1 G
$328.00
About This Item
Linear Formula:
H2C=C(Br)CH2CH2OH
CAS Number:
Molecular Weight:
151.00
Beilstein/REAXYS Number:
1737671
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
98%
form
liquid
refractive index
n20/D 1.499 (lit.)
bp
64-65 °C/9 mmHg (lit.)
density
1.522 g/mL at 25 °C (lit.)
functional group
bromo
hydroxyl
SMILES string
OCCC(Br)=C
InChI
1S/C4H7BrO/c1-4(5)2-3-6/h6H,1-3H2
InChI key
RTKMFQOHBDVEBC-UHFFFAOYSA-N
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General description
3-Bromo-3-buten-1-ol is a primary alcohol. Acetylation of 3-bromo-3-buten-1-ol with acetic acid catalyzed by ytterbium(III) tosylate has been studied.[1]
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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The Journal of Organic Chemistry, 50, 1621-1621 (1985)
Tetrahedron Letters, 27, 3017-3017 (1986)
The Journal of Organic Chemistry, 46, 1723-1723 (1981)
Yen-Pin Lu et al.
Biochemical and biophysical research communications, 379(2), 351-355 (2008-12-24)
Octaprenyl diphosphate synthase (OPPs) and undecaprenyl diphosphate synthases (UPPs) catalyze consecutive condensation reactions of farnesyl diphosphate (FPP) with 5 and 8 isopentenyl diphosphate (IPP) to generate C(40) and C(55) products with trans- and cis-double bonds, respectively. In this study, we
Lanthanide (III) tosylates as new acylation catalysts.
Parac-Vogt TN, et al.
European Journal of Organic Chemistry, 2005(9), 1810-1815 (2005)
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