7492-90-2 Usage
Description
(S)-(+)-1-BROMO-4-METHYLHEXANE is a chemical compound that belongs to the group of alkyl halides. It is a colorless liquid with a strong, pungent odor and is flammable. (S)-(+)-1-BROMO-4-METHYLHEXANE is known for its reactivity and is commonly used in organic synthesis, particularly as a reactant in the production of pharmaceuticals and other specialized chemicals.
Uses
Used in Pharmaceutical Industry:
(S)-(+)-1-BROMO-4-METHYLHEXANE is used as a reactant for the synthesis of various pharmaceuticals. Its reactivity allows for the creation of a wide range of compounds with potential medicinal properties.
Used in Chemical Industry:
(S)-(+)-1-BROMO-4-METHYLHEXANE is used as a solvent in various chemical reactions and industrial processes. Its ability to dissolve a variety of substances makes it a valuable component in the production of specialized chemicals.
Used in Organic Synthesis:
(S)-(+)-1-BROMO-4-METHYLHEXANE is used as a building block in organic synthesis, enabling the creation of complex molecules with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 7492-90-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7492-90:
(6*7)+(5*4)+(4*9)+(3*2)+(2*9)+(1*0)=122
122 % 10 = 2
So 7492-90-2 is a valid CAS Registry Number.
7492-90-2Relevant articles and documents
Selective Aliphatic C-H Oxidation
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Page/Page column 15, (2011/02/18)
A composition including a complex of a metal, a tetradentate ligand, at least one ancillary ligand, and a counterion may be used for selective sp3 C—H bond oxidation. The tetradentate ligand may include a N-heterocyclic-N,N′-bis(pyridyl)-ethane-1,2-diamine group or a N,N′-bis(heterocyclic)-N,N′-bis(pyridyl)-ethane-1,2-diamine group. The composition can be used in combination with H2O2 to effect highly selective oxidations of unactivated sp3 C—H bonds over a broad range of substrates. The site of oxidation can be predicted, based on the electronic and/or steric environment of the C—H bond. In addition, the oxidation reaction does not require the presence of directing groups in the substrate.