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Merck

550337

Sigma-Aldrich

4-氯-3-甲酰基香豆素

97%

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About This Item

经验公式(希尔记法):
C10H5ClO3
CAS号:
分子量:
208.60
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

97%

mp

126-130 °C (lit.)

官能基

aldehyde
chloro
ester

SMILES 字串

[H]C(=O)C1=C(Cl)c2ccccc2OC1=O

InChI

1S/C10H5ClO3/c11-9-6-3-1-2-4-8(6)14-10(13)7(9)5-12/h1-5H

InChI 密鑰

CLLLQUGVEQADNN-UHFFFAOYSA-N

相关类别

一般說明

4-Chloro-3-formylcoumarin, also known as 4-chloro-2-oxo-2H-chromene-3-carbaldehyde, is a coumarin derivative.

應用

4-Chloro-3-formylcoumarin may be used as a reactant in the preparation of:
  • 2-aryl[1]benzopyrano[4,3-c]pyrazol-4(2H)-ones
  • biaryl lactones (benzo[c]chromen-6-ones)
  • N-monosubstituted 4-amino-3-formylcoumarins
  • chromeno[4,3-b]quinolin-6-one

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Synthesis of 6H-benzo [c] chromen-6-ones by cyclocondensation of 1,3-dicarbonyl compounds with 4-chloro-3-formylcoumarin.
Iaroshenko, VO, et al.
Tetrahedron Letters, 52(45), 5910-5912 (2011)
An efficient ultrasound promoted catalyst-free protocol for the synthesis of chromeno [4,3-b] quinolin-6-ones.
Prasad JV, et al.
Chemical Science, 123(5), Prasad JV-Prasad JV (2011)
Reactions of 4-Chloro-3-formylcoumarin with Arylhydrazines.
Strakova I, et al.
Chemistry of Heterocyclic Compounds, 39(12), 1608-1616 (2003)
Reactions of 4-chloro-3-formyl-coumarin with primary amines.
Strakova I, et al.
Chemistry of Heterocyclic Compounds, 42(5), 574-582 (2006)
One-Pot Synthesis of Biaryl Lactones by Sonogashira Cross-Coupling Reactions of 4-Chloro-3-formylcoumarin and Subsequent Domino [5+1] Cyclization/Deacetylation Reactions with 1, 3-Dicarbonyl Compounds.
Iaroshenko VO, et al.
Advanced Synthesis & Catalysis, 354(5), 803-806 (2012)

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