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Sigma-Aldrich

3-Bromo-3-buten-1-ol

98%

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About This Item

Linear Formula:
H2C=C(Br)CH2CH2OH
CAS Number:
Molecular Weight:
151.00
Beilstein:
1737671
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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.)

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.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Panshin SY.
US Geological Survey Data Series (1997)
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)
The Journal of Organic Chemistry, 50, 1621-1621 (1985)
The Journal of Organic Chemistry, 46, 1723-1723 (1981)

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