Skip to Content
MilliporeSigma
All Photos(2)

Documents

410888

Sigma-Aldrich

3-Bromo-3-buten-1-ol

98%

Sign Into View Organizational & Contract Pricing


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

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

signalword

Danger

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


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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

The Journal of Organic Chemistry, 46, 1723-1723 (1981)
The Journal of Organic Chemistry, 50, 1621-1621 (1985)
Tetrahedron Letters, 27, 3017-3017 (1986)
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)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service