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Merck

305847

Sigma-Aldrich

二氢-4,4-二甲基-2,3-呋喃二酮

97%

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About This Item

经验公式(希尔记法):
C6H8O3
CAS号:
分子量:
128.13
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

形狀

solid

mp

67-69 °C (lit.)

溶解度

dichloromethane: soluble 25 mg/mL, clear, colorless to yellow

SMILES 字串

CC1(C)COC(=O)C1=O

InChI

1S/C6H8O3/c1-6(2)3-9-5(8)4(6)7/h3H2,1-2H3

InChI 密鑰

HRTOQFBQOFIFEE-UHFFFAOYSA-N

一般說明

二氢-4,4-二甲基-2,3-呋喃酮是一种活化的酮化合物,它的对映选择性氢化已被报道。中性铑(I)氨基膦-次膦酸酯络合物催化二氢-4,4-二甲基-2,3-呋喃二酮的不对称氢化已被报道。二氢-4,4-二甲基-2,3-呋喃二酮的不对称氢化可生成D-(-)-泛酰基内酯,一种泛酸合成中的关键中间体。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Neutral Rhodium (I) Aminophosphine-Phosphinite Complexes: Synthesis, Structure, and Use in Catalytic Asymmetric Hydrogenation of Activated Keto Compounds.
Agbossou F, et al.
Organometallics, 14(5), 2480-2489 (1995)
S Shimizu et al.
European journal of biochemistry, 174(1), 37-44 (1988-05-16)
A novel enzyme which specifically catalyzes the reduction of conjugated polyketones was purified to homogeneity from cells of Mucor ambiguus AKU 3006. The enzyme has a strict requirement for NADPH and irreversibly reduces a number of quinones such as p-benzoquinone
Rhodium (I) bis (aminophosphane) complexes as catalysts for asymmetric hydrogenation of activated ketones.
Roucoux A, et al.
Tetrahedron Asymmetry, 7(2), 379-382 (1996)
Organic Syntheses, 63, 18-18 (1985)
Norberto Bonalumi et al.
Journal of the American Chemical Society, 125(44), 13342-13343 (2003-10-30)
The combination of ATR-IR and modulation spectroscopy allowed for the study of the interaction of ketopantolactone with Pt/Al2O3 films chirally modified by cinchonidine under hydrogenation conditions. The spectra reveal a significant influence of ketopantolactone on the adsorption of the modifier

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