6343-65-3 Usage
Description
(2S)-2-nitrobicyclo[2.2.1]heptane is a bicyclic compound with a nitro group attached to one of the carbon atoms in the ring. It has a chiral center, with the (2S) configuration indicating that the nitro group is attached to the second carbon atom in the ring in the S configuration. (2S)-2-nitrobicyclo[2.2.1]heptane is of interest in chemical research and development due to its unique structure and chiral nature.
Uses
Used in Organic Synthesis:
(2S)-2-nitrobicyclo[2.2.1]heptane is used as a building block in organic synthesis for the creation of more complex chemical compounds. Its unique structure and chiral nature make it a valuable component in the synthesis of various organic molecules.
Used in Chemical Research and Development:
(2S)-2-nitrobicyclo[2.2.1]heptane is used as a target in chemical research and development due to its potential applications in creating new and innovative chemical compounds. Its unique structure and chiral nature provide opportunities for further exploration and discovery in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 6343-65-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6343-65:
(6*6)+(5*3)+(4*4)+(3*3)+(2*6)+(1*5)=93
93 % 10 = 3
So 6343-65-3 is a valid CAS Registry Number.
6343-65-3Relevant articles and documents
SRN1 reactions in the nitrobenzo[1,3]dioxole series
Meuche-Albeny,Rathelot,Crozet,Vanelle
, p. 989 - 997 (2007/10/03)
5-Chloromethyl-6-nitrobenzo[1,3]dioxole has been shown to react with 2-nitropropane anion to give C-alkylation by an SRN1 mechanism. The reaction was extended to various aliphatic, cyclic, and heterocyclic nitronate anions, leading to a new series of nitrobenzo[1,3]dioxole derivatives.
S(RN)1 synthesis of new 5-nitroimidazoles highly active against protozoa and anaerobes
Vanelle,Crozet,Maldonado,Barreau
, p. 167 - 178 (2007/10/02)
1-Methyl-2-chloromethyl-5-nitroimidazole reacts by an S(RN)1 mechanism with various aliphatic, cyclic or heterocyclic nitronate anions to afford, in high yields, new 5-nitroimidazoles bearing a trisubstituted ethylenic double bond at the 2 position. Some of these compounds are as active as metronidazole in vitro and in vivo against protozoa and anaerobic bacteria. Structure-activity relationships are discussed.
Oxidation of Primary Amines by Dimethyldioxirane
Murray, Robert W.,Rajadhyaksha, Shirish N.,Mohan, Lily
, p. 5783 - 5788 (2007/10/02)
Dimethyldioxirane oxidizes primary amines rapidly, and generally in high yield, to the corresponding nitro compounds.The method can also be used to syntesize polynitro compounds.