14371-82-5 Usage
General Description
2-Nitro-4-(trifluoromethyl)thiophenol is a specialized chemical compound that belongs to the class of organic compounds known as nitrobenzenes. Nitrobenzenes are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a nitro group attached to it. 2-NITRO-4-(TRIFLUOROMETHYL)THIOPHENOL is characterized by a nitro group (-NO2) and a trifluoromethyl group (-CF3) attached to a thiophenol molecule. Thiophenol is a type of phenol where a sulfur atom is directly attached to the benzene ring. The presence of these groups gives the molecule unique chemical properties. Its trifluoromethyl group increases its reactivity and stability, and its nitro group allows it to participate in a variety of chemical reactions. However, detailed information about its physical properties, uses, or toxicity is not readily available and it doesn't have a very common application but is primarily used in the field of organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 14371-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,7 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14371-82:
(7*1)+(6*4)+(5*3)+(4*7)+(3*1)+(2*8)+(1*2)=95
95 % 10 = 5
So 14371-82-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H4F3NO2S/c8-7(9,10)4-1-2-6(14)5(3-4)11(12)13/h1-3,14H
14371-82-5Relevant articles and documents
One-pot synthesis and asymmetric oxidation of 2-nitro-4-(trifluoromethyl) benzene containing sulfides
Rodygin, Konstantin S.,Rubtsova, Svetlana A.,Kutchin, Alexander V.,Slepukhin, Pavel A.
experimental part, p. 1885 - 1894 (2011/10/11)
An efficient one-pot method for the preparation of 2-nitro-4- (trifluoromethyl)benzene containing sulfides from 1,1'-disulfanediylbis[2-nitro- 4-(trifluoromethyl)benzene] is proposed. The corresponding enantiomerically enriched sulfoxides with up to 78% enantiomeric excess are prepared by the asymmetric oxidation of sulfides using a modified Sharpless method. The yield of sulfoxides is shown to decrease with an increase in the bulk of the aliphatic group and with a decrease of the inductive effect of the hydrocarbonic moiety on the sulfur atom. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. Taylor & Francis Group, LLC.
