19780-44-0 Usage
General Description
4-Ethyl-3-hexanol is a colorless liquid with a faint, sweet odor that is used as a fragrance ingredient and solvent. It is a primary alcohol with a six-carbon chain and an ethyl group attached to the third carbon. This chemical is commonly found in perfumes and other personal care products due to its pleasant aroma. It is also used as a solvent in various industrial applications, including the production of other chemicals and in the manufacturing of plastics. 4-Ethyl-3-hexanol is flammable and should be handled with care to avoid potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 19780-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,8 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19780-44:
(7*1)+(6*9)+(5*7)+(4*8)+(3*0)+(2*4)+(1*4)=140
140 % 10 = 0
So 19780-44-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H18O/c1-4-7(5-2)8(9)6-3/h7-9H,4-6H2,1-3H3/t8-/m0/s1
19780-44-0Relevant articles and documents
Modular counter-Fischer?indole synthesis through radical-enolate coupling
Chung, Hyunho,Kim, Jeongyun,Gonzalez-Montiel, Gisela A.,Cheong, Paul Ha-Yeon,Lee, Hong Geun
supporting information, p. 1096 - 1102 (2021/01/26)
A single-electron transfer mediated modular indole formation reaction from a 2-iodoaniline derivative and a ketone has been developed. This transition-metal-free reaction shows a broad substrate scope and unconventional regioselectivity trends. Moreover, important functional groups for further transformation are tolerated under the reaction conditions. Density functional theory studies reveal that the reaction proceeds by metal coordination, which converts a disfavored 5-endo-trig cyclization to an accessible 7-endo-trig process.
