3-Nitrobenzaldehyde

From Wikipedia, the free encyclopedia
(Redirected from 3-nitrobenzaldehyde)
Jump to navigation Jump to search

<templatestyles src="Chembox/styles.css"/>

Template:Chembox AllOtherNamesTemplate:Chembox headerbarTemplate:Chembox SolubilityInWaterTemplate:Chembox headerbarTemplate:Chembox IndexlistTemplate:Chembox JmolTemplate:Chembox ChEMBLTemplate:Chembox ECHATemplate:Chembox E numberTemplate:Chembox IUPHAR ligandTemplate:Chembox UNIITemplate:Chembox CompToxTemplate:Chembox headerbarTemplate:Chembox OHS (set)Template:Chembox GHS (set)Template:Chembox Datapage checkTemplate:Chembox Footer
3-Nitrobenzaldehyde[1][2]
Template:Chembox image sbs cell
Template:Longitem Template:Chembox Elements/molecular formula
Molar mass Template:Chem molar mass
Appearance Yellowish to brownish crystalline powder or granulate
Melting point Template:Chembox CalcTemperatures
Boiling point Template:Chembox CalcTemperatures
Template:Longitem −68.55·10−6 cm3/mol
Template:Longitem Template:Unbulleted list
ChEBI Template:Unbulleted list
ChemSpider Template:Unbulleted list
DrugBank Template:Unbulleted list
EC Number Template:Unbulleted list
KEGG Template:Unbulleted list
Template:Longitem Template:Unbulleted list
RTECS number Template:Unbulleted list
Script error: No such module "collapsible list".
Script error: No such module "collapsible list".
NFPA 704 (fire diamond) Template:NFPA 704 diamond

Template:Chembox Footer/trackingScript error: No such module "TemplatePar".Template:Short description

3-Nitrobenzaldehyde is an organic compound with the formula Template:Chem2. It is one of three isomers of nitrobenzaldehyde. It contains a nitro group meta-substituted to the aldehyde.

3-Nitrobenzaldehyde is the primary product obtained via the mono-nitration of benzaldehyde with nitric acid.[3]

Template:Chem2

Product distribution is about 19% for the ortho-, 72% for the meta- and 9% for the para isomers.

Uses

3-Nitrobenzaldehyde is a precursor to the drug Tipranavir. It is a mainstay in the synthesis of Dihydropyridine calcium channel blockers. Via selective reduction of the nitro group, it is a precursor to the diazonium salt.[4]

References

  1. ↑ 3-Nitrobenzaldehyde
  2. ↑ Script error: No such module "citation/CS1".
  3. ↑ Script error: No such module "citation/CS1".
  4. ↑ Script error: No such module "Citation/CS1".