85351-07-1 Usage
Uses
Used in Pharmaceutical Industry:
3-Methyldodecanonitrile is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicinal compounds.
Used in Pesticide Industry:
In the pesticide industry, 3-Methyldodecanonitrile serves as a key intermediate, aiding in the production of effective and targeted pest control agents.
Used in Flavor and Fragrance Industry:
3-Methyldodecanonitrile is utilized as a component in the creation of flavors and fragrances, enhancing the sensory attributes of various consumer products.
Used in Organic Compounds Synthesis:
This chemical compound is employed as an intermediate in the synthesis of a range of organic compounds, broadening its applications across different chemical and industrial processes.
Used in Industrial and Laboratory Settings:
3-Methyldodecanonitrile is used as a reagent or solvent in various chemical reactions and processes, facilitating the production and manipulation of different substances in a controlled environment.
Check Digit Verification of cas no
The CAS Registry Mumber 85351-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,5 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85351-07:
(7*8)+(6*5)+(5*3)+(4*5)+(3*1)+(2*0)+(1*7)=131
131 % 10 = 1
So 85351-07-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H25N/c1-3-4-5-6-7-8-9-10-13(2)11-12-14/h13H,3-11H2,1-2H3
85351-07-1Relevant academic research and scientific papers
Electrochemical Tandem Olefination and Hydrogenation Reaction with Ammonia
Zhang, Xiaofeng,Jiang, Runze,Cheng, Xu
, p. 16016 - 16025 (2021/08/24)
An electrochemical Horner-Wadsworth-Emmons/hydrogenation tandem reaction was achieved using ammonia as electron and proton donors. The reaction could give two-carbon-elongated ester and nitrile from aldehyde or ketones directly. This reaction could proceed with a catalytic amount of base or even without a base. The ammonia provides both the electron and proton for this tandem reaction and enables the catalyst-free hydrogenation of an α,β-unsaturated HWE intermediate. More than 40 examples were reported, and functional groups, including heterocycles and hydroxyl, were tolerated.
Ketone precursors for organoleptic compounds
-
, (2008/06/13)
The invention discloses ketones of formula I: wherein, Y is an optionally substituted alkyl, cycloalkyl, or cycloalkylalkyl, wherein each alkyl group is straight or branched and each alkyl and cycloalkyl group is saturated or unsaturated; R1is hydrogen or a C1-6alkyl group that is substituted, saturated or unsaturated, straight or branched; A is a chromophoric substituted aromatic ring or ring system; n is an integer; and with the proviso that formula I is not 2-ethoxy-1-phenyl-ethanone. These compositions are useful for the delivery of organoleptic compounds, especially of flavors, fragrances, masking agents and antimicrobial compounds.
