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Merck
CN

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
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
249-763-3
MDL number:
Assay:
98%
Form:
solid
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assay

98%

form

solid

bp

105 °C/15 mmHg (lit.)

mp

50-52 °C (lit.)

functional group

aldehyde

SMILES string

[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

Application

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


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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



全球贸易项目编号

货号GTIN
264598-5G04061826123232