3613-33-0 Usage
Uses
Used in the Food Industry:
Octanal, 7-ethoxy-3,7-dimethylis used as a flavoring agent for its strong, fruity odor, enhancing the taste and aroma of various food products.
Used in Cleaning and Personal Care Products:
Leveraging its potent antimicrobial properties, Octanal, 7-ethoxy-3,7-dimethylis incorporated into cleaning and personal care products to ensure hygiene and prevent microbial growth.
Used in Perfume and Fragrance Production:
Octanal, 7-ethoxy-3,7-dimethylis utilized in the production of perfumes and fragrances, contributing to their pleasant and appealing scents.
Used in Chemical Synthesis and Industrial Processes:
Octanal, 7-ethoxy-3,7-dimethylis also employed in the synthesis of other organic compounds and plays a crucial role in a variety of chemical and industrial processes, highlighting its importance in the broader field of chemistry and manufacturing.
Check Digit Verification of cas no
The CAS Registry Mumber 3613-33-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,1 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3613-33:
(6*3)+(5*6)+(4*1)+(3*3)+(2*3)+(1*3)=70
70 % 10 = 0
So 3613-33-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H24O2/c1-5-14-12(3,4)9-6-7-11(2)8-10-13/h10-11H,5-9H2,1-4H3
3613-33-0Relevant academic research and scientific papers
PREPARATION OF DERIVATIVES OF CITRONELLAL
Koertvelyessy, Gyula
, p. 347 - 354 (2007/10/02)
The hydrogenation of citronellal and citral, if not separated from ethereal oils, leads regioselectively to dihydrocitronellal and citronellal, respectively.The reaction of citral with (+)-ephedrin or L-aspartic acid, followed by hydrogenation and deblocking the aldehyde function, yields optically active citronellal.Reacting the aldehyde function of citronellal with diethanolamine, piperidine or morpholine, the alcohol addition to the 6,7-double bond results in 7-alkoxy substituted citronellals with acceptable yield.The formation of 7-hydroxy-6,7-dihydrocitronellal during this reaction has been proved and the effect of reaction parameters on the yield have been discussed.
Studies on Potential Juvenile Hormone Analogs: Part II - Synthesis of Some New Ethers, Schiff Bases, Hydrazides and Hydrazones Derived from 7-Hydroxycitronellal
Gupta, Anurag Ateet,Rastogi, Anita,Gupta, M. M.,Srivastava, Neera,Sengupta, A. K.,Athar, Mohd
, p. 948 - 951 (2007/10/02)
A number of ethers, schiff bases, hydrazides and hydrazones derived from 7-hydroxycitronellal hyve been synthesized and tested on common Indian red cotton bug (Dysdercus koenigii) for JH activity.Only compounds 2 and 9 show marginal activity.
