CN
检测方案
97%
折射率
n20/D 1.578 (lit.)
bp
98 °C/9.5 mmHg (lit.)
密度
1.042 g/mL at 25 °C (lit.)
储存温度
2-8°C
SMILES string
CN(C)\N=C\c1ccco1
InChI
1S/C7H10N2O/c1-9(2)8-6-7-4-3-5-10-7/h3-6H,1-2H3/b8-6+
InChI key
DURWBNUASAZMSN-SOFGYWHQSA-N
一般描述
Combined matrix isolation FTIR and theoretical DFT(B3LYP)/6-311++G(d,p) study of 2-furaldehyde dimethylhydrazone has been reported.
应用
2-Furaldehyde dimethylhydrazone (2-furaldehyde N,N-dimethylhydrazone) has been used in the preparation of:
- furyl-1,4-quinone and hydroquinones by reaction with benzo- and naphthoquinones
- dimethylaminohydrazonofurylquinones
法规信息
新产品
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示例
T1503
货号
-
25G
包装规格/数量
其它示例：
705578-5MG-PW
PL860-CGA/SHF-1EA
MMYOMAG-74K-13
1000309185
输入内容 1.000309185)
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Julio Benites et al.
Investigational new drugs, 29(5), 760-767 (2010-03-20)
We describe the biological activity of some furylbenzo- and naphthoquinones (furylquinones) on hepatocarcinoma cells and healthy rat liver slices. The effects of furylquinones on cancer cells (Transplantable Liver Tumor, TLT) were assessed by measuring cell death (membrane cell lysis); intracellular
Julio Benites et al.
Bioorganic & medicinal chemistry, 16(2), 862-868 (2007-10-30)
The preparation of furyl-1,4-quinone and hydroquinones by reaction of 2-furaldehyde N,N-dimethylhydrazone with benzo- and naphthoquinones is reported. Access to furylnaphthoquinones from unactivated quinones requires acid-induced conditions, however oxidative coupling reactions of activated quinones proceed under neutral conditions. The in vitro
C Araujo-Andrade et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 97, 830-837 (2012-08-21)
In this work, a combined matrix isolation FTIR and theoretical DFT(B3LYP)/6-311++G(d,p) study of 2-furaldehyde dimethylhydrazone (2FDH) was performed. According to calculations, two E and two Z conformers exist, the E forms having considerably lower energy than the Z forms. The
P Rao et al.
Analytical biochemistry, 189(2), 178-181 (1990-09-01)
Even though the chromogens formed from mannose and galactose showed comparable absorbances at 480 nm in the conventional (developer present during heat of dilution) and modified (developer reacted at room temperature after cooling; epsilon mannose = 13,700, galactose = 14,000)
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