130850
3-丁炔-1-醇
97%
别名:
3-Butynol
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关于此项目
线性分子式:
HC≡CCH2CH2OH
化学文摘社编号:
分子量:
70.09
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39020335
UNSPSC Code:
12352100
EC Number:
213-161-9
MDL number:
Beilstein/REAXYS Number:
773710
产品名称
3-丁炔-1-醇, 97%
InChI key
OTJZCIYGRUNXTP-UHFFFAOYSA-N
InChI
1S/C4H6O/c1-2-3-4-5/h1,5H,3-4H2
SMILES string
OCCC#C
assay
97%
form
liquid
refractive index
n20/D 1.441 (lit.)
bp
128.9 °C (lit.)
mp
−63.6 °C (lit.)
density
0.926 g/mL at 25 °C (lit.)
functional group
hydroxyl
Quality Level
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Application
3-丁炔-1-醇用于制备马氏加成物 。
合成元用于制备含氧杂环 和受保护的s-羟基-L-异亮氨酸酯
在钯催化偶合 β-tetrionic酸溴化物的研究中，使用炔基底物，可使生成炔基取代呋喃酮的产量很高。
General description
3-丁炔-1-醇的燃烧和汽化焓用静态燃烧量热法和相关气相色谱法测量 。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
96.8 °F - closed cup
flash_point_c
36 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Tetrahedron Letters, 48, 105-105 (2007)
Kopf, Henning; Pietraszuk. et al.
Organometallics, 25(10), 2533-2546 (2006)
Sumod A Pullarkat et al.
Inorganic chemistry, 45(18), 7455-7463 (2006-08-29)
Alcohol functionalized diphosphine ligands with chirality residing on the carbon backbone were prepared using a novel two-stage asymmetric synthetic methodology from the corresponding terminal alkynols. Under mild conditions, the alkynols, 3-butyn-1-ol and 2-propyn-1-ol, were subjected to direct hydrophosphination to give
Ederley Vélez et al.
The journal of physical chemistry. A, 109(34), 7832-7838 (2006-07-13)
The enthalpies of combustion and vaporization of 3-buten-1-ol and 3-butyn-1-ol have been measured by static bomb combustion calorimetry and correlation gas chromatography techniques, respectively, and the gas-phase enthalpies of formation, Delta(f)H degrees (m)(g), have been determined, the values being -147.3
Kristen Bennett et al.
Applied and environmental microbiology, 82(8), 2270-2279 (2016-01-31)
Nitrosomonas europaea is an aerobic nitrifying bacterium that oxidizes ammonia (NH3) to nitrite (NO2 (-)) through the sequential activities of ammonia monooxygenase (AMO) and hydroxylamine dehydrogenase (HAO). Many alkynes are mechanism-based inactivators of AMO, and here we describe an activity-based
商品
Alkynes' versatility enables reactions like addition, metathesis, hydroboration, cleavage, coupling, and cycloadditions in synthetic chemistry.
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