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About This Item
Linear Formula:
CH3C≡CCH2OH
CAS Number:
Molecular Weight:
70.09
Beilstein:
1733676
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
liquid
refractive index
n20/D 1.453 (lit.)
bp
142-143 °C (lit.)
mp
−2.2 °C (lit.)
density
0.937 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
CC#CCO
InChI
1S/C4H6O/c1-2-3-4-5/h5H,4H2,1H3
InChI key
NEEDEQSZOUAJMU-UHFFFAOYSA-N
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Application
2-Butyn-1-ol was used in the synthesis of homocoupling products, [{Ru(P(OCH3)3)2(CH3CN)3}2{μ-SCRCHCH(OCH2CCR)S}](CF3SO3)4.
Synthesis of macrocyclic ethers via metathesis reactions of cyclohexanes and cyclohexenes with allylic and propargylic side chains.†
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
123.8 °F - closed cup
Flash Point(C)
51 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Kazuko Matsumoto et al.
Journal of the American Chemical Society, 124(44), 13106-13113 (2002-10-31)
A variety of inter- and intramolecular dehydration was found in the reactions of [[Ru(P(OCH(3))(3))(2)(CH(3)CN)(3)](2)(mu-S(2))](CF(3)SO(3))(4) (1) with hydroxyl substituted alkenes and alkynes. Treatment of 1 with allyl alcohol gave a C(3)S(2) five-membered ring complex, [[Ru(P(OCH(3))(3))(2)(CH(3)CN)(3)](2)[mu-SCH(2)CH(2)CH(OCH(2)CH=CH(2))S]](CF(3)SO(3))(4) (2), via C-S bond formation after
European Journal of Organic Chemistry, 3727-3727 (2007)
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