31367-46-1 Usage
Uses
Used in Perfume and Flavor Industry:
3-Methyl-2-heptanol is used as a solvent for the production of perfumes and flavors, providing a stable and effective medium for the blending and extraction of aromatic compounds.
Used in Chemical Products Industry:
3-Methyl-2-heptanol serves as a solvent in the manufacture of various chemical products, including plasticizers, lubricants, and detergents, due to its ability to dissolve a wide range of substances.
Used in Pharmaceutical Industry:
3-Methyl-2-heptanol is used as a chemical intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and medications.
Used in Agrochemical Industry:
3-Methyl-2-heptanol is utilized in the production of agrochemicals, such as pesticides and herbicides, as a chemical intermediate, enabling the creation of effective agricultural products.
Check Digit Verification of cas no
The CAS Registry Mumber 31367-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,3,6 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31367-46:
(7*3)+(6*1)+(5*3)+(4*6)+(3*7)+(2*4)+(1*6)=101
101 % 10 = 1
So 31367-46-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H18O/c1-4-5-6-7(2)8(3)9/h7-9H,4-6H2,1-3H3
31367-46-1Relevant academic research and scientific papers
Stereochemistry of Aliphatic Carbocations, 13. Protonated Cyclopropanes as Intermediates in 1,2-Alkyl Shifts
Kirmse, Wolfgang,Loosen, Karin,Prolingheuer, Ernst-Christoph
, p. 129 - 141 (2007/10/02)
The nitrous acid deamination of 2-ethyl-1-methylbutylamine (10), 1,2-diethylbutylamine (35), and 2-ethyl-1-methylpentylamine (43) has been studied with respect to 1,2-alkyl shifts.Optically active and deuterated amines were employed whenever possible.The structure, configuration, and deuterium distribution of various products (e. g. 16 from 10, 40 and 48 from 35, 56 from 43) are most reasonably explained in terms of alkyl-bridged intermediates (corner-protonated cyclopropanes) which isomerize via proton shifts from corner to corner.The alternative interconversion of open ions via 1,3-H shifts is incompatible with our experimental results.