1160-74-3 Usage
Uses
Used in Organic Chemistry:
1-[1-[2-(2,4-Dinitrophenyl)hydrazono]ethyl]cyclohexane is used as a reagent in organic chemistry for the formation of other organic compounds due to its hydrazone group, which can participate in various chemical reactions.
Used in Dye and Colorant Industry:
1-[1-[2-(2,4-Dinitrophenyl)hydrazono]ethyl]cyclohexane is used as a potential dye or colorant in the dye and colorant industry, leveraging the 2,4-dinitrophenyl group that may impart color properties to materials.
Used in Materials Science:
1-[1-[2-(2,4-Dinitrophenyl)hydrazono]ethyl]cyclohexane is used in materials science for its potential applications in the development of new materials or as a precursor for the synthesis of other cyclohexane derivatives, given the presence of the cyclohexane ring.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, the compound's complex structure and functional groups may also suggest potential uses in the pharmaceutical industry as a starting material for the development of new drugs or drug candidates, particularly if its chemical properties can be harnessed for medicinal chemistry applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1160-74-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,6 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1160-74:
(6*1)+(5*1)+(4*6)+(3*0)+(2*7)+(1*4)=53
53 % 10 = 3
So 1160-74-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N4O4/c1-10(11-5-3-2-4-6-11)15-16-13-8-7-12(17(19)20)9-14(13)18(21)22/h7-9,11,16H,2-6H2,1H3
1160-74-3Relevant academic research and scientific papers
New Methods and Reagents in Organic Synthesis; 73. Trimethylsilyldiazomethane: A Convenient Reagent for the Conversion of Aliphatic Aldehydes to the Homologous Methyl Ketones
Aoyama, Toyohiko,Shioiri, Takayuki
, p. 228 - 229 (2007/10/02)
Trimethylsilyldiazomethane reacts smoothly with aliphatic aldehydes in the presence of magnesium bromide (1.5 eqiv) to give homologous methyl ketones after direct treatment with 10percent hydrochloric acid/methanol (1:1).
