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Heliotropin, also known as Piperazine vanillin or Piperazine ethanone, is a chemical compound with a strong, sweet, floral scent reminiscent of heliotrope flowers. It is used as a fragrance ingredient in various products, including perfumes, cosmetics, and soaps. Heliotropin is a white crystalline solid with the chemical formula C10H20N2O and a molecular weight of 184.28 g/mol. It is synthesized by reacting vanillin with piperazine, and its chemical structure consists of a vanillin moiety attached to a piperazine ring. Heliotropin is considered safe for use in fragrances, but it may cause skin irritation or allergic reactions in some individuals. It is important to note that "Heliotropin Iso-Butyrate" is not a recognized chemical compound, and it is likely a misnomer or a typo. The correct term is "Heliotropin," which is the chemical compound discussed above.

461-08-5

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461-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 461-08-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 461-08:
(5*4)+(4*6)+(3*1)+(2*0)+(1*8)=55
55 % 10 = 5
So 461-08-5 is a valid CAS Registry Number.
InChI:InChI=1/C3F6S3/c4-2(5,6)11-1(10)12-3(7,8)9

461-08-5Relevant academic research and scientific papers

Reactions of trifluoromethylthiocopper with halomethanes

Munavalli,Rossman,Rohrbaugh,Ferguson,Durst

, p. 7 - 13 (2007/10/03)

The reaction of trifluoromethylthiocopper with halomethanes, namely di-and triiodo-, dibromodichloro-, dibromochlorofluoro-, dibromo-difluoro-, bromochlorofluoro-, phenyltrichloro-, bromocyano-and dibromofluoro-methanes, has been investigated in detail. In addition to the expected compounds, the formation of unusual products such as bis (trifluoromethyl) trithiocarbonate, dimethyl (trifluoromethylthio) benzene, bis (trifluoromethylthio) fluoromethane, (trifluoromethylthio) carbonyl fluoride, carbon disulfide, carbon tetrachloride, trifluoromethylthio-benzoate, etc. was observed. In some cases, bis (trifluoromethylthio) mercury has been used instead of trifluoromethylthiocopper. The mechanism of formation of the various products and their mass spectral fragmentation behavior are described.

Synthesis and biological screening of trifluoromethylthioarsenicals

Munavalli, S.,Rossman, D. I.,Rohrbaugh, D. K.,Ferguson, C. P.,Buettner, L.

, p. 15 - 20 (2007/10/02)

The title compounds have been prepared from the reaction of trifluoromethylthiocopper and alkyl mono- and di-haloarsines.This communication describes their synthesis, biological screening and mass spectral fragmentation behavior.

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