62987-05-7 Usage
Description
FD 1 is a chemical compound that belongs to the class of aphrodisiacs, known for its aromatic and mood-boosting properties. It is commonly used in the production of perfumes and fragrances, as well as in aromatherapy products due to its potential mood-enhancing effects. However, its use may be restricted in certain applications due to the possibility of causing allergic reactions in sensitive individuals.
Uses
Used in Perfume and Fragrance Industry:
FD 1 is used as a key ingredient in perfumes and fragrances for its aromatic properties, contributing to the overall scent and enhancing the appeal of these products.
Used in Aromatherapy Products:
FD 1 is used as a mood-enhancing agent in aromatherapy products, aiming to improve the emotional well-being of individuals through its scent.
Used in Cosmetics Industry:
FD 1 is used in various cosmetics products for its aphrodisiac properties, potentially boosting the mood and attractiveness of the users.
Check Digit Verification of cas no
The CAS Registry Mumber 62987-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,8 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62987-05:
(7*6)+(6*2)+(5*9)+(4*8)+(3*7)+(2*0)+(1*5)=157
157 % 10 = 7
So 62987-05-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H15FN2O4/c13-8-7-14(9-3-1-5-18-9)12(17)15(11(8)16)10-4-2-6-19-10/h7,9-10H,1-6H2
62987-05-7Relevant articles and documents
Synthesis of Tegafur by the Alkylation of 5-Fluorouracil under the Lewis Acid and Metal Salt-Free Conditions
Zasada, Aleksandra,Mironiuk-Puchalska, Ewa,Koszytkowska-Stawińska, Mariola
, p. 885 - 889 (2017/06/23)
A novel protocol for preparation of tegafur (a prodrug of 5-fluorouracil) is reported. The process involves the 1,8-diazabicycloundec-7-ene-mediated alkylation of 5-fluorouracil with 2-acetoxytetrahydrofuran at 90 °C, followed by treatment of the prepurified mixture of the alkylation products with aqueous ethanol at 70 °C. The yield of the two-step process is 72%.
5-Fluorouracil derivatives. X. Synthesis and antitumor activities of α-alkoxyalkyl-5-fluorouracils
Ozaki,Watanabe,Hoshiko,Nagase,Ogasawara,Furukawa,Uemura,Ishikawa,Mori
, p. 150 - 157 (2007/10/02)
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Process for producing 5-fluorouracil derivative with a calcium chloride catalyst
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, (2008/06/13)
5-Fluorouracil derivative having the formula STR1 wherein R represents hydrogen atom or 2-tetrahydrofuryl group is produced by reacting more than equi-mole of 2,3-dihydrofuran with 5-fluorouracil in a polar aprotic solvent with a catalytically effective amount of a catalyst selected from the group consisting of metal halides, non-metal halides, tertiary amine salt of inorganic acids and organic acids in neutral or basic condition at 50° to 150° C under pressure.