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Merck
CN

19170

3-Buten-1-ol

purum, ≥98.0% (GC)

Synonym(s):

Allylcarbinol

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About This Item

Linear Formula:
CH2=CHCH2CH2OH
CAS Number:
627-27-0
Molecular Weight:
72.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329751827
EC Number:
210-991-3
Beilstein/REAXYS Number:
1633504
MDL number:
MFCD00002959

Key Documents

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Product Name

3-Buten-1-ol, purum, ≥98.0% (GC)

InChI key

ZSPTYLOMNJNZNG-UHFFFAOYSA-N

InChI

1S/C4H8O/c1-2-3-4-5/h2,5H,1,3-4H2

SMILES string

OCCC=C

grade

purum

assay

≥98.0% (GC)

refractive index

n20/D 1.421 (lit.)
n20/D 1.422

bp

112-114 °C (lit.)

density

0.838 g/mL at 25 °C (lit.)

functional group

allyl
hydroxyl

Quality Level

100

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Application

3-Buten-1-ol was used as a starting reagent in asymmetric total synthesis of natural seimatopolide B. It was also used in the synthesis of catalytic bimetallic nanoparticles.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

91.4 °F - closed cup

flash_point_c

33 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCBP1862V

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Biologically programmed synthesis of bimetallic nanostructures.
Slocik JM and Naik RR.
Advanced Materials, 18(15), 1988-1992 (2006)
Alternating copolymers of functional alkenes with carbon monoxide.
Kacker S, et al.
Macromolecules, 29(18), 5852-5858 (1996)
Chada Raji Reddy et al.
Organic & biomolecular chemistry, 11(20), 3355-3364 (2013-04-09)
The asymmetric total synthesis of natural seimatopolide B along with its enantiomer is described starting from readily available 5-hexen-1-ol and 3-buten-1-ol. The key steps involved are Jacobson hydrolytic kinetic resolution, proline-catalyzed α-hydroxylation, Yamaguchi esterification and ring-closing metathesis. This asymmetric total

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