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Merck
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重要文件

264598

Sigma-Aldrich

1,4-苯并二噁烷-6-甲醛

98%

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About This Item

經驗公式(希爾表示法):
C9H8O3
CAS號碼:
分子量::
164.16
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

形狀

solid

bp

105 °C/15 mmHg (lit.)

mp

50-52 °C (lit.)

官能基

aldehyde

SMILES 字串

[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 密鑰

CWKXDPPQCVWXAG-UHFFFAOYSA-N

應用

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

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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分析證明 (COA)

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Structure-activity relationships involving the catechol subunit of rolipram.
Stafford JA, et al.
Bioorganic & Medicinal Chemistry Letters, 4(15), 1855-1860 (1994)
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.
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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