326487-53-0

Basic information

• Product Name: 1-NITRO-4-(OCT-1-YNYL)BENZENE
• Synonyms: 1-NITRO-4-(OCT-1-YNYL)BENZENE
• CAS NO: 326487-53-0
• Molecular Formula: C₁₄H₁₇NO₂
• Molecular Weight: 231.29028
• Mol File: 326487-53-0.mol
• Article Data: 23

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-NITRO-4-(OCT-1-YNYL)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-NITRO-4-(OCT-1-YNYL)BENZENE(326487-53-0)
• EPA Substance Registry System: 1-NITRO-4-(OCT-1-YNYL)BENZENE(326487-53-0)

Safety Data

• Hazardous Substances Data: 326487-53-0(Hazardous Substances Data)

Usage

Nitro compound

1-NITRO-4-(OCT-1-YNYL)BENZENE contains a nitro group (-NO2) a functional group consisting of one nitrogen atom and two oxygen atoms.

Benzene ring

The compound contains a benzene ring, which is a six-membered aromatic ring with alternating single and double bonds between carbon atoms.

Nitro group position

The nitro group is attached to the 1-position of the benzene ring, which refers to the first carbon atom in the ring.

Oct-1-ynyl group

The compound contains an oct-1-ynyl group (a straight-chain alkyl group with one triple-bonded carbon atom) at the 4-position of the benzene ring.

Organic intermediates

1-NITRO-4-(OCT-1-YNYL)BENZENE is used in the production of various organic intermediates, which are compounds that are used to synthesize other chemicals.

Pharmaceutical and agrochemical synthesis

The compound is used as a building block for the synthesis of pharmaceuticals and agrochemicals, which are chemicals used in the production of medicines and pesticides, respectively.

Dyes, pigments, and specialty chemicals

1-NITRO-4-(OCT-1-YNYL)BENZENE is also used in the manufacturing of dyes, pigments, and other specialty chemicals.

Hazardous chemical

1-NITRO-4-(OCT-1-YNYL)BENZENE is considered to be a hazardous chemical, and proper safety precautions should be taken when handling and storing it to prevent accidents and exposure.

Upstream product

• 629-05-0 n-octyne 
• 586-78-7 para-nitrophenyl bromide 
• 636-98-6 p-nitrobenzene iodide 
• 16967-02-5 1-phenyl-1-octyne 
• 100-00-5 4-chlorobenzonitrile 

Downstream Products

• 1432044-12-6 4-(4-nitrophenyl)undec-1-en-5-one 
• 1432044-11-5 2-allyl-1-(4-nitrophenyl)octan-1-one 
• 16245-79-7 4-octylaniline 
• 1260137-21-0 N-(2-chloroethyl)-4-octylaniline 
• 1260137-20-9 2-chloro-N-(4-octylphenyl)ethanamide 
• 1260137-22-1 1-(4-octylphenyl)aziridine 
• 1260137-24-3 tert-butyl 2-(4-octylphenylamino)acetate 

Relevant articles and documents

Facile synthesis of Pd nanoparticles supported on a novel Schiff base modified chitosan-kaolin: Antibacterial and catalytic activities in Sonogashira coupling reaction

The present work studies the Sonogashira coupling reaction (SCR) between aryl halides and acetylenes under aerobic conditions using the catalytic complex of Pd nanoparticles (NPs) supported on a novel Schiff base modified chitosan-kaolin (Pd NPs@CS-Kao) in ethanol solvent. The prepared catalyst was characterized by TEM, SEM, FT-IR, XRD, EDS, XPS, elemental mapping, and Raman analyses. The products were formed in high yields. At the end of the reaction, Pd NPs@CS-Kao can be filtered and reused for five consecutive cycles. The advantages of this catalytic process include simple methodology, high yields, and easy work-up. In addition, Pd NPs@CS-Kao exhibited effective antibacterial performance against E. coli gram-negative bacteria.

Pd nanoparticles loaded on modified chitosan-Unye bentonite microcapsules: A reusable nanocatalyst for Sonogashira coupling reaction

This work investigates the preparation of a catalytic complex of palladium nanoparticles supported on novel Schiff base modified chitosan-Unye bentonite microcapsules (Pd NPs@CS-UN). The complex has been characterized by FT-IR, EDS, XRD, TEM, HRTEM, Raman

Efficient Sonogashira and A3 coupling reactions catalyzed by biosynthesized magnetic Fe3O4@Ni nanoparticles from Euphorbia maculata extract

In this work, biosynthesized Fe3O4@Ni nanoparticles using Euphorbia maculata aqueous have been used as effective catalysts in the synthesis of 2,3-disubstituted benzo[b]furan derivatives using three component coupling of aldehydes, s