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重要文件

464643

Sigma-Aldrich

1-Cbz-4-哌啶酮

99%

同義詞:

1-苄氧羰基-4-哌啶酮, N-CBZ-4-哌啶酮, N-苄氧羰基-4-哌啶酮

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About This Item

經驗公式(希爾表示法):
C13H15NO3
CAS號碼:
分子量::
233.26
Beilstein:
1533716
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

99%

折射率

n20/D 1.542 (lit.)

bp

114-140 °C/0.25 mmHg (lit.)

密度

1.172 g/mL at 25 °C (lit.)

官能基

ketone
phenyl

SMILES 字串

O=C1CCN(CC1)C(=O)OCc2ccccc2

InChI

1S/C13H15NO3/c15-12-6-8-14(9-7-12)13(16)17-10-11-4-2-1-3-5-11/h1-5H,6-10H2

InChI 密鑰

VZOVOHRDLOYBJX-UHFFFAOYSA-N

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象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral - Aquatic Chronic 3

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

235.4 °F - closed cup

閃點(°C)

113 °C - closed cup

個人防護裝備

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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Yong Huang et al.
Journal of the American Chemical Society, 124(33), 9662-9663 (2002-08-15)
We report the first examples of hydrogen-bond-promoted acceleration of hetero-Diels-Alder reactions and the use of such catalysis for the hetero-Diels-Alder reactions of simple, unactivated ketones. Several spiro-fused dihydropyans were synthesized in good yields using this procedure. This activation protocol represents
Synthesis, 325-325 (2006)
Iyassu K Sebhat et al.
Journal of medicinal chemistry, 45(21), 4589-4593 (2002-10-04)
Synthetic and natural peptides that act as nonselective melanocortin receptor agonists have been found to be anorexigenic and to stimulate erectile activity. We report the design and development of 1, a potent, selective (1184-fold vs MC3R, 350-fold vs MC5R), small-molecule
Tetrahedron Letters, 42, 6943-6943 (2001)
Biheteroaromatic diphosphine oxides-catalyzed stereoselective direct aldol reactions.
Rossi S, et al.
Tetrahedron, 67(1), 158-166 (2011)

文章

Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

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