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Merck
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399299

Sigma-Aldrich

反-4-甲氧基-β-硝基苯乙烯

99%

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About This Item

線性公式:
CH3OC6H4CH=CHNO2
CAS號碼:
分子量::
179.17
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

99%

mp

86-88 °C (lit.)

溶解度

chloroform: soluble 25 mg/mL, clear, yellow

SMILES 字串

[H]\C(=C(\[H])[N+]([O-])=O)c1ccc(OC)cc1

InChI

1S/C9H9NO3/c1-13-9-4-2-8(3-5-9)6-7-10(11)12/h2-7H,1H3/b7-6+

InChI 密鑰

JKQUXSHVQGBODD-VOTSOKGWSA-N

一般說明

trans-4-Methoxy-β-nitrostyrene participates in the Michael reaction on carbapenam intermediate.

應用

trans-4-Methoxy-β-nitrostyrene acts as guest molecule and forms guest molecules forming co-crystal phases with the d-form of robust syndiotactic polystyrene (sPS). It may be employed as a Michael acceptor in the synthesis of proline based chiral ionic liquid catalysts with two five-membered unsaturated aza-heterocycles.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

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

dust mask type N95 (US), Eyeshields, Gloves


分析證明 (COA)

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Polymer co-crystalline films for photonics.
Daniel C, et al.
Journal of the European Optical Society: Rapid Publications, 4 (2009)
Proline Based Chiral Ionic Liquids for Enantioselective Michael Reaction.
Nobuoka K, et al.
Organic Chemistry International (2014)
Sachin A Pawar et al.
Organic & biomolecular chemistry, 11(48), 8294-8297 (2013-11-13)
Herein, we report the development of mild, organocatalyzed routes to novel carbapenam derivatives through aldol, Mannich and Michael C-C bond forming reactions.

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