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Dear Customer:

The current international situation is complex and volatile, and uncertain tariff policies may potentially impact our product prices. Given these uncertainties, we value your understanding regarding order-related matters.

If you decide to place an order during this period, we reserve the right to adjust the price based on the evolving situation. We understand that market changes may cause inconvenience. We will negotiate with you if there’s a significant price fluctuation due to tariff policy changes before the order’s actual delivery, and in such cases we may adjust or cancel the order as necessary.

Merck
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主要文件

668540

Sigma-Aldrich

(2S,5S)-(–)-5-苄基-3-甲基-2-(5-甲基-2-呋喃基)-4-咪唑烷酮

95%

别名:

(2S,5S)-3-甲基-2-(5-甲基-2-呋喃基)-5-(苯甲基)-4-咪唑烷酮

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25 MG
CN¥1,956.58

CN¥1,956.58


预计发货时间June 16, 2025详情


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25 MG
CN¥1,956.58

About This Item

经验公式(希尔记法):
C16H18N2O2
分子量:
270.33
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22

CN¥1,956.58


预计发货时间June 16, 2025详情


获取大包装报价

质量水平

方案

95%

折射率

n20/D 1.5598

官能团

phenyl

SMILES字符串

CN1[C@H](N[C@@H](Cc2ccccc2)C1=O)c3ccc(C)o3

InChI

1S/C16H18N2O2/c1-11-8-9-14(20-11)15-17-13(16(19)18(15)2)10-12-6-4-3-5-7-12/h3-9,13,15,17H,10H2,1-2H3/t13-,15-/m0/s1

InChI key

IQIMPHPFMHVWBZ-ZFWWWQNUSA-N

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此商品
M2070178488189497
Merbarone A cell-permeable anticancer drug that inhibits the catalytic activity of topoisomerase II (topo II) without damaging DNA or stabilizing DNA-topo II cleavable complexes.

445800

Merbarone

Merbarone ≥98% (HPLC), solid

M2070

Merbarone

form

solid

form

solid

form

solid

form

solid

manufacturer/tradename

Calbiochem®

manufacturer/tradename

-

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

Quality Level

100

Quality Level

-

Quality Level

100

Quality Level

100

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

solubility

DMSO: 100 mg/mL

solubility

DMSO: >5 mg/mL

solubility

DMSO: 100 mg/mL, ethanol: 20 mg/mL

solubility

DMSO: 50 mg/mL

应用

用于和简单 α,β-不饱和酮发生 Diels-Alder 反应的高选择性有机催化剂。[1]
Catalyst for:
  • Enantioselective organocatalytic transfer hydrogenation of cycloalkenones with tert-Bu Hantzsch ester as source of hydrogen
  • Alkylation of indoles with an α,β-disubstituted α,β-unsaturated aldehyde in the enantioselective preparation of a selective serotonin reuptake inhibitor
  • MacMillan reaction

法律信息

适用美国专利 6,369,243 和相关专利。仅供研究使用。

象形图

Skull and crossbones

警示用语:

Danger

危险分类

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

>230.0 °F

闪点(°C)

> 110 °C

个人防护装备

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


  • 历史批次信息供参考:

    分析证书(COA)

    Lot/Batch Number

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    Burk, M. J. et al
    Journal of the American Chemical Society, 118, 5142-5142 (1996)

    商品

    Discover Professor David MacMillan's groundbreaking metal-free asymmetric catalysis using imidazolidinone-based organocatalysts for versatile transformations.

    我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

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