99096-59-0 Usage
Description
(3R)-(-)-Linalyl-β-D-glucopyranosid is a natural chemical compound consisting of a linalool molecule bound to a glucose molecule. It is found in various plants and is known for its pleasant floral scent. This versatile compound has potential uses in multiple industries due to its unique properties.
Uses
Used in Perfumery Industry:
(3R)-(-)-Linalyl-β-D-glucopyranosid is used as a fragrance ingredient for its floral scent, contributing to the overall aroma of perfumes.
Used in Food and Beverage Industry:
(3R)-(-)-Linalyl-β-D-glucopyranosid is used as a flavoring agent to enhance the taste and aroma of various food and beverage products.
Used in Pharmaceutical Industry:
(3R)-(-)-Linalyl-β-D-glucopyranosid is used as a potential medicinal compound for its anti-inflammatory and antioxidant effects, and is being studied for its application in the development of new drugs.
Used in Cosmetic Industry:
(3R)-(-)-Linalyl-β-D-glucopyranosid is used as a natural ingredient in cosmetics for its pleasant scent and potential skin care benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 99096-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,0,9 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 99096-59:
(7*9)+(6*9)+(5*0)+(4*9)+(3*6)+(2*5)+(1*9)=190
190 % 10 = 0
So 99096-59-0 is a valid CAS Registry Number.
99096-59-0Relevant articles and documents
First total synthesis of two new diglycosides, neohancosides A and B, from Cynanchum hancockianum
Konda, Yaeko,Toida, Tsuneyuki,Kaji, Eisuke,Takeda, Kazuyoshi,Harigaya, Yoshihiro
, p. 123 - 143 (2007/10/03)
Neohancosides A (1) and B (2) are monoterpene diglycosides isolated from Cynanchum hancockianum, which is a Chinese folk medicine having antitumor activity. First total synthesis of 1 and 2, (3R)-linaloyl and (3R)-8-hydroxylinaloyl 3-O-β-D-xylopyranosyl-(1 → 6)-β-D-glucopyranosides were achieved stereoselectively using fluoride 12b as a glycosyl donor. The asymmetry of C-3 in 1 and 2 was introduced efficiently by separating diasteremers of (3R), (3S)-linaloyl and (3R), (3S)-8-benzoyloxylinaloyl 3-O-2,3,4-tri-O-benzoyl-β-D-glucopyranoside, 19 and 21 and 20 and 22, respectively. Absolute configurations of 1 and 2 were determined by enzymatic degradation of synthetic intermediates 33 and 34.
Synthesis of Glycosides of Mono-, Sesqui-, and Diterpene Alcohols
Paulsen, Hans,Le-Nguyen, Bien,Sinnwell, Volker,Heemann, Volker,Seehofer, Friedlieb
, p. 1513 - 1536 (2007/10/02)
The β-D-glucopyranosides of the monoterpene alcohols (S)-(-)-β-citronellol (1), (S)-cis-verbenol (5), (3R)-(-)-linalool (8), dihydromyrcenol (11), terpinen-4-ol (14), of the norcarotionoides β-ionol (17), α-ionol (22), and of the sesquiterpene alcohol (+)
