B103209
2-Butyne-1,4-diol
99%
동의어(들):
1,4-Butynediol, 1,4-Dihydroxy-2-butyne, 2-Butynediol, Bis(hydroxymethyl)acetylene
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모든 사진(4)
About This Item
Linear Formula:
HOCH2C≡CCH2OH
CAS Number:
Molecular Weight:
86.09
Beilstein:
1071237
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
vapor pressure
<0.1 mmHg ( 55 °C)
Quality Level
분석
99%
양식
crystals
bp
238 °C (lit.)
mp
53-58 °C (lit.)
SMILES string
OCC#CCO
InChI
1S/C4H6O2/c5-3-1-2-4-6/h5-6H,3-4H2
InChI key
DLDJFQGPPSQZKI-UHFFFAOYSA-N
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관련 카테고리
애플리케이션
2-Butyne-1,4-diol is extensively used in the cycloaddition reactions such as the homologation method for the preparation of substituted acenes, rhodium and iridium-catalyzed [2+ 2+ 2] inter and intramolecular cyclotrimerization. It can also be used in the total synthesis of (−)-isolaurallene, (−)-amphidinolide P and bistramide A.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT RE 2
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 2
Flash Point (°F)
305.6 °F - closed cup
Flash Point (°C)
152 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
A highly efficient and flexible synthesis of substituted carbazoles by rhodium?catalyzed inter?and intramolecular alkyne cyclotrimerizations.
Witulski B and Alayrac C
Angewandte Chemie (International Edition in English), 114(17), 3415-3418 (2002)
Asymmetric total synthesis of (?)-isolaurallene.
Crimmins M T and Emmitte K A
Journal of the American Chemical Society, 123(7), 1533-1534 (2001)
Total synthesis of (?)-amphidinolide P.
Williams D R, et al.
Organic Letters, 2(7), 945-948 (2000)
Homologation method for preparation of substituted pentacenes and naphthacenes.
Takahashi T, et al.
The Journal of Organic Chemistry, 71(21), 7967-7977 (2006)
Synthesis of silafluorenes by iridium-catalyzed [2+ 2+ 2] cycloaddition of silicon-bridged diynes with alkynes.
Matsuda T, et al.
Organic Letters, 9(1), 133-136 (2007)
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