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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide

4-BROMO-5-NITRO-ISOQUINOLINE-1-CARBALDEHYDE synthesis

5synthesis methods
Isoquinoline, 4-bromo-1-methyl-5-nitro-

171880-55-0
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4-BROMO-5-NITRO-ISOQUINOLINE-1-CARBALDEHYDE

171880-56-1
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Yield:171880-56-1 55%

Reaction Conditions:

with selenium(IV) oxide in 1,4-dioxane; for 3 h;Heating;

References:

Liu, Mao-Chin;Lin, Tai-Shun;Penketh, Philip;Sartorelli, Alan C. [Journal of Medicinal Chemistry,1995,vol. 38,# 21,p. 4234 - 4243]

4-Bromoisoquinoline

1532-97-4
349 suppliers
$14.00/10g

4-BROMO-5-NITRO-ISOQUINOLINE-1-CARBALDEHYDE

171880-56-1
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References
4-BROMO-ISOQUINOLINE 2-OXIDE

3749-21-1
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4-BROMO-5-NITRO-ISOQUINOLINE-1-CARBALDEHYDE

171880-56-1
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References
4-BROMO-1-METHYL-ISOQUINOLINE

104704-40-7
39 suppliers
$103.00/100mg

4-BROMO-5-NITRO-ISOQUINOLINE-1-CARBALDEHYDE

171880-56-1
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References
Acetic acid, 2-(4-bromo-1(2H)-isoquinolinylidene)-2-cyano-, ethyl ester

171880-20-9
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4-BROMO-5-NITRO-ISOQUINOLINE-1-CARBALDEHYDE

171880-56-1
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References

4-BROMO-5-NITRO-ISOQUINOLINE-1-CARBALDEHYDE Related Search:

ISOQUINOLINE-1-CARBALDEHYDE