6750-30-7 Usage
Uses
Used in Pharmaceutical Industry:
Arnidiol is used as a potential triterpenoid for anti-viral activity against SARS-CoV-2 and related Coronaviruses. Its unique chemical structure allows it to interact with viral proteins and inhibit their replication, providing a potential therapeutic option for treating viral infections.
Used in Cosmetic Industry:
Glycerol is used as a humectant in cosmetic products, such as creams, lotions, and moisturizers, to help retain moisture in the skin and prevent dryness. Its hygroscopic properties make it an effective ingredient for maintaining skin hydration and improving skin texture.
Used in Food Industry:
Glycerol is used as a sweetener, preservative, and humectant in various food products. It can be found in baked goods, confectionery, and beverages, where it helps to improve texture, extend shelf life, and enhance taste.
Used in Personal Care Industry:
Glycerol is used in personal care products, such as toothpaste, mouthwashes, and shaving creams, to provide lubrication, improve texture, and maintain moisture balance.
Used in Industrial Applications:
Glycerol is used in various industrial applications, such as in the production of biodiesel, as a component in the manufacturing of certain types of resins and plastics, and as a solvent in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 6750-30-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,5 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6750-30:
(6*6)+(5*7)+(4*5)+(3*0)+(2*3)+(1*0)=97
97 % 10 = 7
So 6750-30-7 is a valid CAS Registry Number.
InChI:InChI=1/C30H50O2/c1-18-11-14-28(6)24(32)17-30(8)20(25(28)19(18)2)9-10-22-27(5)15-13-23(31)26(3,4)21(27)12-16-29(22,30)7/h19-25,31-32H,1,9-17H2,2-8H3/t19-,20-,21+,22?,23+,24+,25+,27+,28-,29-,30-/m1/s1
6750-30-7Relevant academic research and scientific papers
Terpenoids in four Inula species from Bulgaria
Aneva, Ina,Ivanova, Victoria,Staleva, Plamena,Todorova, Milka,Trendafilova, Antoaneta
, p. 1229 - 1240 (2022/02/16)
Phytochemical study of the chloroform extract of the aerial parts of Inula germanica L., I. ensifolia L., I. conyza (Griess.) DC. and I. salicina L. led to the identification of 33 terpenoids. β- and α-amyrin, lupeol, taraxasterol, ψ-taraxasterol and their 3-O-acetates and 3-O-palmitates were identified by GC/MS. In addition, the structures of 3-O-palmitates of mainaladiol, arnidiol, faradiol and 16-hydroxylupeol were confirmed by NMR. ent-Kaur-16-en-19- -oic acid and its 15α-(3-methylpentanoyloxy) and 15α-(3-methylbutanoyloxy) derivatives were isolated from I. conyza. Ten closely related sesquiterpene lactones (germacranolides and melampolides) were found in I. germanica and their structural identification was performed by spectral analyses. I. ensifolia and I. salicina were free of sesquiterpene lactones and diterpenoids. All triterpenoids and diterpenoids, grazielia acid, desacetylovatifolin and 8-(2-methylbutanoyloxy)- 1(10),4,11(13)-germacrutrien-6,12-olide-14-oic acid are described for the first time in the studied species. The principal component analysis was used to find a relationship between the investigated up to now Inula species, growing in Bulgaria.
