2602-61-1 Usage
Description
N,N-Diethyldecanamide, with the molecular formula C16H33NO, is a chemical compound that serves as a potent insect repellent. It is recognized for its ability to deter a broad spectrum of insects, including mosquitoes, ticks, and fleas, by disrupting their host-seeking capabilities. This effectiveness, coupled with its safety and regulatory approval, positions N,N-Diethyldecanamide as a favored choice for outdoor enthusiasts and in regions where insect-borne diseases are a concern.
Uses
Used in Insect Repellent Products:
N,N-Diethyldecanamide is used as an active ingredient in various commercial insect repellent products for its efficacy in repelling insects. It is favored for outdoor activities and in areas where insect-borne diseases are prevalent, providing protection by interfering with the insect's ability to detect and locate potential hosts.
Used in Public Health and Disease Prevention:
In the context of public health, N,N-Diethyldecanamide is utilized as a critical component in insect repellents to prevent the transmission of insect-borne diseases. Its inclusion in repellent formulations helps in reducing the risk of diseases caused by insects such as malaria, Lyme disease, and Zika virus, thereby playing a significant role in disease prevention strategies.
Used in Regulatory Approved Applications:
N,N-Diethyldecanamide is used in insect repellent formulations that are approved by regulatory agencies such as the Environmental Protection Agency (EPA) in the United States. This approval indicates that the compound meets safety and efficacy standards, ensuring consumers have access to reliable and effective insect repellent products.
Check Digit Verification of cas no
The CAS Registry Mumber 2602-61-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,0 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2602-61:
(6*2)+(5*6)+(4*0)+(3*2)+(2*6)+(1*1)=61
61 % 10 = 1
So 2602-61-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H29NO/c1-4-7-8-9-10-11-12-13-14(16)15(5-2)6-3/h4-13H2,1-3H3
2602-61-1Relevant articles and documents
Iridium-Catalyzed Reductive Strecker Reaction for Late-Stage Amide and Lactam Cyanation
Fuentes de Arriba, ángel L.,Lenci, Elena,Sonawane, Mahendra,Formery, Odilon,Dixon, Darren J.
supporting information, p. 3655 - 3659 (2017/03/21)
A new iridium-catalyzed reductive Strecker reaction for the direct and efficient formation of α-amino nitrile products from a broad range of (hetero)aromatic and aliphatic tertiary amides, and N-alkyl lactams is reported. The protocol exploits the mild and highly chemoselective reduction of the amide and lactam functionalities using IrCl(CO)[P(C6H5)3]2 (Vaska's complex) in the presence of tetramethyldisiloxane, as a reductant, to directly generate hemiaminal species able to undergo substitution by cyanide upon treatment with TMSCN (TMS=trimethylsilyl). The protocol is simple to perform, broad in scope, efficient (up to 99 % yield), and has been successfully applied to the late-stage functionalization of amide- and lactam-containing drugs, and naturally occurring alkaloids, as well as for the selective cyanation of the carbonyl carbon atom linked to the N atom of proline residues within di- and tripeptides.
Nickel-catalyzed cross-coupling of unactivated alkyl halides and tosylate carrying a functional group with alkyl and phenyl Grignard reagents
Singh, Surya Prakash,Terao, Jun,Kambe, Nobuaki
experimental part, p. 5644 - 5646 (2011/02/25)
By the use of catalytic amounts of a nickel salt and a 1,3-butadiene, primary and secondary alkyl Grignard reagents undergo cross-coupling with alkyl bromides, iodide, and tosylate carrying a functional group such as amide, ester, and ketone at 0 °C in THF. The present procedure provides a simple, convenient, and practical method for construction of carbon chains in the presence of various functional groups. PhMgBr also gave the corresponding coupling product in a moderate yield.
Facile Homologation of N,N-Dialkyl-α-bromoacetamide by Trialkylboranes in the Presence of Lithium Diisopropylamide
Li, Nan-Sheng,Deng, Min-Zhi,Huang, Yao-Zeng
, p. 6118 - 6119 (2007/10/02)
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