264598
1,4-苯并二噁烷-6-甲醛
98%
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关于此项目
经验公式（希尔记法）:
C9H8O3
化学文摘社编号:
分子量:
164.16
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
方案
98%
表单
solid
沸点
105 °C/15 mmHg (lit.)
mp
50-52 °C (lit.)
官能团
aldehyde
SMILES字符串
[H]C(=O)c1ccc2OCCOc2c1
InChI
1S/C9H8O3/c10-6-7-1-2-8-9(5-7)12-4-3-11-8/h1-2,5-6H,3-4H2
InChI key
CWKXDPPQCVWXAG-UHFFFAOYSA-N
应用
1,4-苯并二噁烷-6-甲醛已用于：
- 作为结构单元合成四氢异喹啉酮
- 制备苯并呋喃类似物，作为CAMP特异性IV型磷酸二酯酶的潜在抑制剂
- 合成(5Z)-5-(2,3-二氢-1,4-苯并二噁烷-6-基亚甲基)-1-甲基-2-硫酮咪唑啉-4-酮
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Khadidja Bourahla et al.
Molecules (Basel, Switzerland), 16(9), 7377-7390 (2011-09-01)
A practical protocol for the preparation of (5Z)-2-alkylthio-5-arylmethylene-1-methyl-1,5-dihydro-4H-imidazol-4-one derivatives is reported. The new compounds were obtained in good yield and stereoselectivity in two steps, namely a solvent-free Knoevenagel condensation under microwave irradiation, followed by an S-alkylation reaction with various halogenoalkanes.
Structure-activity relationships involving the catechol subunit of rolipram.
Stafford JA, et al.
Bioorganic & Medicinal Chemistry Letters, 4(15), 1855-1860 (1994)
M Lebl
Bioorganic & medicinal chemistry letters, 9(9), 1305-1310 (1999-05-26)
A new technique for high throughput solid phase synthesis using the centrifuge based liquid removal from readily available standard microtiterplates is described. This technique eliminates the filtration step and is therefore applicable to simultaneous processing of an unlimited number of
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