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Merck
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文件

115282

Sigma-Aldrich

间苯二甲醛

97%

别名:

1,3-苯二甲醛

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About This Item

线性分子式:
C6H4-1,3-(CHO)2
CAS号:
626-19-7
分子量:
134.13
Beilstein:
1561038
EC號碼:
210-935-8
MDL號碼:
MFCD00003372
分類程式碼代碼:
12352100
PubChem物質ID:
24847208
NACRES:
NA.22

化驗

97%

mp

87-88 °C (lit.)

SMILES 字串

O=Cc1cccc(C=O)c1

InChI

1S/C8H6O2/c9-5-7-2-1-3-8(4-7)6-10/h1-6H

InChI 密鑰

IZALUMVGBVKPJD-UHFFFAOYSA-N

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相关类别

一般說明

间苯二甲醛参与碱催化的 Knoevenagel 缩合反应。

應用

间苯二甲醛用于双核钉联吡啶络合物的合成。

包裝

玻璃瓶封装

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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The effect of outer-sphere acidity on chemical reactivity in a synthetic heterogeneous base catalyst.
John D Bass et al.
Angewandte Chemie (International ed. in English), 42(42), 5219-5222 (2003-11-06)
Johanna Andersson et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 16(36), 11037-11046 (2010-08-04)
The binuclear ruthenium complex [μ-bidppz(phen)(4)Ru(2)](4+) has been extensively studied since the discovery of its unusual threading intercalation interaction with DNA, a binding mode with extremely slow binding and dissociation kinetics. The complex has been shown to be selective towards long

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Knoevenagel Condensation Reaction

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 Reaction

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 Reaction

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 Reaction

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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