CAS 7244-77-1
:1-Nitro-4-propoxybenzene
Description:
1-Nitro-4-propoxybenzene, with the CAS number 7244-77-1, is an organic compound characterized by the presence of a nitro group (-NO2) and a propoxy group (-O-CH2-CH2-CH3) attached to a benzene ring. This compound typically appears as a pale yellow to light brown liquid or solid, depending on its purity and temperature. It is known for its aromatic properties, which contribute to its stability and reactivity. The nitro group is an electron-withdrawing substituent, influencing the compound's reactivity in electrophilic aromatic substitution reactions. The propoxy group, being an ether, can enhance the solubility of the compound in organic solvents. 1-Nitro-4-propoxybenzene may be used in various applications, including as an intermediate in organic synthesis and in the production of dyes or pharmaceuticals. Safety precautions should be observed when handling this compound, as nitro compounds can be hazardous and may pose environmental risks.
Formula:C9H11NO3
InChI:InChI=1S/C9H11NO3/c1-2-7-13-9-5-3-8(4-6-9)10(11)12/h3-6H,2,7H2,1H3
InChI key:InChIKey=AWOXUNCNGSHHSP-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=CC=C(OCCC)C=C1
Synonyms:- 1-Nitro-4-Propoxybenzene
- 4-Nitrophenyl propyl ether
- Benzene, 1-nitro-4-propoxy-
- Ether, p-nitrophenyl propyl
- Propyl p-nitrophenyl ether
- p-Nitropropoxybenzene
- p-Propoxynitrobenzene
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Found 2 products.
1-Nitro-4-propoxybenzene
CAS:1-Nitro-4-propoxybenzene is a covalent inhibitor of aspartic acid proteases. It is an aspartic acid analog that competes with the natural substrate for the active site and inhibits the transpeptidation reaction. This compound has been shown to be highly selective against renin, which is a key enzyme in the blood coagulation cascade. The 1-nitro group can be replaced by other groups to modulate potency or selectivity. These modifications may also improve water solubility, stability, or bioavailability.
Formula:C9H11NO3Purity:Min. 95%Molecular weight:181.19 g/mol
