244430
3-Hexyn-1-ol
98%
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About This Item
Linear Formula:
C2H5C≡CCH2CH2OH
CAS Number:
Molecular Weight:
98.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
213-685-8
MDL number:
Assay:
98%
Form:
liquid
Product Name
3-Hexyn-1-ol, 98%
InChI key
ODEHKVYXWLXRRR-UHFFFAOYSA-N
InChI
1S/C6H10O/c1-2-3-4-5-6-7/h7H,2,5-6H2,1H3
SMILES string
CCC#CCCO
assay
98%
form
liquid
refractive index
n20/D 1.454 (lit.)
bp
63-64 °C/12 mmHg (lit.)
density
0.898 g/mL at 25 °C (lit.)
functional group
hydroxyl
Quality Level
Related Categories
General description
The stereoselective hydrogenation of 3-hexyn-1-ol was studied. Poly(N-vinyl-2-pyrrolidone)-stabilized Pd-nanoclusters showed an extraordinary catalytic performance in the selective hydrogenation of 3-hexyn-1-ol.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
145.4 °F - closed cup
flash_point_c
63 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Jules C A A Roelofs et al.
Chemical communications (Cambridge, England), (8)(8), 970-971 (2004-04-08)
Poly(N-vinyl-2-pyrrolidone)-stabilized Pd-nanoclusters, for the first time exclusively supported on the hydrotalcite lateral surface, showed a remarkable catalytic performance in the selective hydrogenation of 3-hexyn-1-ol, which can be ascribed to both the influence of the protecting polymer PVP as well as
Alexander Sachse et al.
Dalton transactions (Cambridge, England : 2003), 42(5), 1378-1384 (2012-10-12)
Well-dispersed Pd nanoparticles have been synthesized inside the mesoporosity of a silica monolith featuring hierarchical porosity of homogeneous interconnected macropores (4 microns) and mesopores (11 nm). These monoliths have been implemented as microreactors for selective hydrogenation reactions. Conversion and selectivity
Shigeru Tamogami et al.
FEBS letters, 589(3), 390-395 (2015-01-13)
The medicinal herbal plant Achyranthes bidentata (A. bidentata) produces the sweet-odor ester - methyl (E)-2-hexenoate (1) as the major volatile in response to methyl jasmonate (MeJA). Here, we investigated the biosynthetic pathway of methyl (E)-2-hexenoate (1). The common plant precursor
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