CAS 1734-79-8

4-Nitrocinnamaldehyde

Description:

4-Nitrocinnamaldehyde is an organic compound characterized by its aromatic structure, featuring a nitro group and an aldehyde functional group. It is a yellow crystalline solid at room temperature, exhibiting a melting point that varies based on purity and specific conditions. The compound is known for its distinctive odor and is soluble in organic solvents such as ethanol and acetone, but has limited solubility in water. Its chemical formula is C10H9NO3, indicating the presence of a phenyl ring, a double bond between the carbon atoms, and the aldehyde functional group. 4-Nitrocinnamaldehyde is often utilized in organic synthesis and as a building block in the preparation of various pharmaceuticals and agrochemicals. Additionally, it exhibits interesting photophysical properties, making it a subject of study in materials science and photochemistry. Due to the presence of the nitro group, it may also display some degree of reactivity, particularly in electrophilic substitution reactions. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled.

Formula: C₉H₇NO₃

InChI: InChI=1S/C9H7NO3/c11-7-1-2-8-3-5-9(6-4-8)10(12)13/h1-7H

InChI key: InChIKey=ALGQVMMYDWQDEC-UHFFFAOYSA-N

SMILES: N(=O)(=O)C1=CC=C(C=CC=O)C=C1

Synonyms:

• (E)-3-(4-nitrophenyl)prop-2-enal
• (Z)-3-(4-nitrophenyl)prop-2-enal
• 2-Propenal, 3-(4-nitrophenyl)-
• 3-(4-Nitrophenyl)-2-propenal
• 3-(4-Nitrophenyl)acrolein
• 3-(4-Nitrophenyl)acrylaldehyde
• 4-Nitrocinnamaldahyde
• 4-Nitrocinnamic aldehyde
• Brn 1565424
• Ccris 3774
• Cinnamaldehyde, p-nitro-
• Nsc 1318
• p-Nitrocinnamaldehyde

(E)-4-Nitrocinnamaldehyde

CAS: 1734-79-8, 49678-08-2

Formula: C₉H₇NO₃

Purity: >98.0%(GC)

Color and Shape: Light yellow to Brown to Dark green powder to crystal

Molecular weight: 177.16

Ref: 3B-N0541

3-(4-Nitrophenyl);acrylaldehyde

CAS: 1734-79-8

Formula: C₉H₇NO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 177.1568

Ref: IN-DA001YVL

3-(4-Nitrophenyl)acrylaldehyde

CAS: 1734-79-8

3-(4-Nitrophenyl)acrylaldehyde

Purity: 97%

Molecular weight: 177.16g/mol

Ref: 54-OR1002111

4-Nitrocinnamaldehyde

CAS: 1734-79-8

4-Nitrocinnamaldehyde is a diazonium salt that is used as an efficient method for the synthesis of nitro compounds. Nitro compounds are used in the production of explosives, insecticides, and herbicides. 4-Nitrocinnamaldehyde reacts with hydrochloric acid to produce trifluoroacetic acid, which is then reacted with an organic compound to produce a nitro compound. This reaction has been shown to be irreversible and not sensitive to functional groups. 4-Nitrocinnamaldehyde binds to the enzyme cytochrome P450 reductase, inhibiting its function. The binding of 4-nitrocinnamaldehyde to enzymes such as pyruvate kinase and acetylcholinesterase has also been observed in binding experiments.

Formula: C₉H₇NO₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 177.16 g/mol

Ref: 3D-FN70975

3-(4-Nitrophenyl)acrylaldehyde

CAS: 1734-79-8

Formula: C₉H₇NO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 177.159

Ref: 10-F240494

4-Nitrocinnamaldehyde, predominantly trans, 98%

CAS: 1734-79-8

Doebner-Miller reaction the 4- nitrocinnamaldehyde and 2-methylaniline in concentrated HC1 give the corresponding 8-methyl-2-phenylquinoline (3: R = 4'-N02) directly. The asymmetric Friedel-Crafts-type alkylation in aqueous media reaction of 4-Nitrocinnamaldehydr with N-methyl indole using trifluoro

Formula: C₉H₇NO₃

Purity: 98%

Color and Shape: White to yellow to orange, Powder

Molecular weight: 177.16

Ref: 02-A11467