117-18-0 | Tecnazene

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$25.00	$17.00
5g	95%	in stock	$41.00	$29.00
25g	95%	in stock	$97.00	$68.00
100g	95%	in stock	$297.00	$208.00
500g	95%	in stock	$643.00	$450.00

Description

• Catalog Number: AE08791
• Chemical Name: Tecnazene
• CAS Number: 117-18-0
• Molecular Formula: C6HCl4NO2
• Molecular Weight: 260.8896
• MDL Number: MFCD00007066
• SMILES: Clc1cc(Cl)c(c(c1Cl)[N+](=O)[O-])Cl
• NSC Number: 10235

Computed Properties

• Complexity: 195
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 2
• XLogP3: 3.9

Upstream Synthesis Route

2,3,5,6-Tetrachloronitrobenzene is a versatile compound commonly utilized in chemical synthesis for its reactivity and unique properties. This chemical serves as a valuable building block in the creation of various organic molecules due to its ability to undergo a wide range of reactions.In chemical synthesis, 2,3,5,6-Tetrachloronitrobenzene can be used as a precursor in the preparation of complex aromatic compounds through substitution reactions. The presence of nitro and chloro functional groups in the molecule allows for diverse substitution patterns, enabling the introduction of different functional groups at specific positions on the benzene ring.Furthermore, 2,3,5,6-Tetrachloronitrobenzene can participate in nitration, reduction, and cross-coupling reactions, providing avenues for the synthesis of various intermediates and final products. Its ability to undergo selective transformations under controlled conditions makes it a valuable tool in organic chemistry laboratories for the construction of intricate organic molecules.Overall, 2,3,5,6-Tetrachloronitrobenzene plays a crucial role in chemical synthesis by serving as a key intermediate in the preparation of diverse organic compounds with tailored properties for applications in pharmaceuticals, materials science, and other fields of chemistry.

Literature

• Molecular structure, vibrational spectra, HOMO, LUMO and NMR studies of 1,2-dichloro-4-nitrobenzene and 2,3,5,6-tetrachloro-1-nitrobenzene based on density functional calculations.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20120201

• Permeation of tecnazene through human skin in vitro as assessed by HS-SPME and GC-MS.

  Environmental science & technology 20080901

• Residues of 18 organochlorine pesticides in 30 traditional Chinese medicines.

  Chemosphere 20080401

• Increased scratching counts depend on a decrease in ability of cutaneous prostaglandin D2 biosynthesis in NC/Nga mice with atopic dermatitis.

  Experimental dermatology 20051201

• Scratching behavior in spontaneous- or allergic contact-induced dermatitis in NC/Nga mice.

  Experimental dermatology 20051101

• Studies on TMPD:TCNB; a donor-acceptor with room temperature paramagnetism and n-pi interaction.

  Molecules (Basel, Switzerland) 20040831

• Ion chromatographic determination of the decomposition products of tecnazene solution irradiated by ultraviolet light: inorganic and organic anions.

  Journal of agricultural and food chemistry 20010601