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Benzene, 1-chloro-2-nitro-4-[(trifluoromethyl)thio]-, also known as 1-Chloro-2-nitro-4-(trifluoromethylthio)benzene, is an organic compound with the chemical formula C7H3ClF3NO2S. It is a derivative of benzene, featuring a chlorine atom at the 1st position, a nitro group at the 2nd position, and a trifluoromethylthio group at the 4th position. Benzene, 1-chloro-2-nitro-4-[(trifluoromethyl)thio]- is characterized by its aromatic structure, with the chlorine and nitro groups providing electrophilic properties, while the trifluoromethylthio group introduces a strong electron-withdrawing effect. It is a colorless to pale yellow liquid with a pungent odor and is used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and potential toxicity, it is important to handle Benzene, 1-chloro-2-nitro-4-[(trifluoromethyl)thio]- with care and in accordance with proper safety protocols.

404-73-9

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404-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 404-73-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 404-73:
(5*4)+(4*0)+(3*4)+(2*7)+(1*3)=49
49 % 10 = 9
So 404-73-9 is a valid CAS Registry Number.

404-73-9Downstream Products

404-73-9Relevant academic research and scientific papers

New 4-pentafluorosulfanyl and 4-perfluoroalkylthio derivatives of 1-chloro-2-nitro- and 1-chloro-2,6-dinitrobenzenes

Sipyagin, Alexey M.,Enshov, Vyacheslav S.,Kashtanov, Sergei A.,Bateman, Colin P.,Mullen, Brian D.,Tan, Ying-Teck,Thrasher, Joseph S.

, p. 1305 - 1316 (2007/10/03)

New 4-pentafluorosulfanyl and 4-perfluoroalkylthio derivatives of 1-chloro-2-nitrobenzene and 1-chloro-2,6-dinitrobenzene were prepared from the corresponding bis(4-chloro-3-nitrophenyl)disulfide and bis(4-chloro-3,5-dinitrophenyl)disulfide, respectively. The SF5 derivatives were obtained by fluorination of the disulfides with AgF2 according to Sheppard's method, while perfluoroalkylation was carried out by means of thermolytic reactions with xenon(II) bis(perfluoroalkylcarboxylates). The introduction of fluorine-containing, electron-withdrawing substituents into the aromatic ring (in the presence of other deactivating groups) reinforces the activation of the halogen substituent towards nucleophilic attack. Several nucleophilic substitution reactions have been carried out with these compounds, and as a result, some N- and S-containing groups were introduced in the benzene ring. For example, the previously unknown SF5, CF3S, and C2F5S analogues of trifluralin (Treflan) were prepared and characterized. Additional synthetic possibilities for heterocyclic chemistry are presented on the basis of reactions of the new 1-chloro-2,6-dinitrobenzene derivatives with ethyl thioglycolate wherein fluorine-containing derivatives of benzothiazole N-oxide were obtained as the main products.

Synthesis of aryl perfluoroalkyl sulfides from aromatic disulfides

Sipyagin,Enshov,Kashtanov,Potemkin,Thrasher,Waterfeld

, p. 420 - 434 (2007/10/03)

Thermolysis of xenon(II) bis(perfluoroalkanecarboxylates) in the presence of diaryl disulfides occurs through the S-S bond cleavage to form dihalo-, halonitro-, and halodinitrophenyl perfluoroalkyl sulfides. The latter type of compounds was obtained for the first time. The main side process is the perfluoroalkylation of the aromatic ring.

Heterocyclic compounds

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, (2008/06/13)

The invention provides compounds of formula (I) having nematicidal, insecticidal, acaricidal and fungicidal properties, compositions comprising them and processes and intermediates for their preparation: STR1 wherein: X is oxygen or sulphur; n is 0, 1 or 2; R1, R2, R3, and R4 are as described in the specification.

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