699-61-6 Usage
Description
Cyclohexanepropanoicacid,1-hydroxy-,gamma-lactone, also known as gamma-hydroxy-cyclohexanepropionic acid lactone, is a chemical compound with a cyclic structure that features a lactone group. It is characterized by its sweet, creamy, and coconut-like odor.
Used in Flavor and Fragrance Industry:
Cyclohexanepropanoicacid,1-hydroxy-,gamma-lactone is used as a flavoring agent in the flavor and fragrance industry for its sweet, creamy, and coconut-like odor. It is commonly added to food products to enhance their aroma and taste.
Used in Food Products:
Cyclohexanepropanoicacid,1-hydroxy-,gamma-lactone is used as a flavor enhancer in food products due to its sweet, creamy, and coconut-like odor. It is generally recognized as safe for use in food and can be found in a variety of products.
Used in Cosmetic and Personal Care Products:
Cyclohexanepropanoicacid,1-hydroxy-,gamma-lactone is used as a fragrance ingredient in cosmetic and personal care products. Its sweet, creamy, and coconut-like odor makes it a desirable addition to these products.
Check Digit Verification of cas no
The CAS Registry Mumber 699-61-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 699-61:
(5*6)+(4*9)+(3*9)+(2*6)+(1*1)=106
106 % 10 = 6
So 699-61-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O2/c10-8-4-7-9(11-8)5-2-1-3-6-9/h1-7H2
699-61-6Relevant articles and documents
Samarium (II) iodide-induced intermolecular coupling of a,b-unsaturated esters with ketones: Reactions of methyl propiolate and ethyl buta-2,3-dienoate with cyclohexanone and its application to synthesis of a terpene carboxylic acid
Sono, Masakazu,Doi, Natsuki,Yoshino, Eri,Onishi, Sachiko,Fujii, Daiki,Tori, Motoo
supporting information, p. 1947 - 1950 (2013/04/10)
The reactions of methyl propiolate and ethyl buta-2,3-dienoate with cyclohexanone induced by SmI2 occurred either at a- or b-position to yield different products depending on with or without a proton source. The synthesis of terpenic acid was demonstrated using this reaction.
Homoaldol and aldol reactions from common enolates and oxirance: Reaction of reductively generated chromium enolates through cationic rearrangement
Hojo, Makoto,Sakata, Kyosuke,Maimaiti, Xiamuxikamaer,Ueno, Junya,Nishikori, Hisashi,Hosomi, Akira
, p. 142 - 143 (2007/10/03)
Enolates generated from α-bromo esters by the reduction with Bu6CrLi3 react with oxiranes to afford γ-hydroxy esters and β-hydroxy esters, depending on the Lewis acid used as a promoter.
Samarium diiodide promoted spirolactonization of cycloalkanones
Csuk,Hu,Abdou,Kratky
, p. 7037 - 7044 (2007/10/02)
Reaction of cycloalkanones with methyl 3-bromopropionate and SmI2 afforded formation of spiroanellated γ-lactones, pinacols and unprecedented 3-(1-hydroxycycloalkyl)-1-oxaspiro[n,m]alkan-2-ones.