35050-88-5 Usage
Description
2,6-Diethyl-4-methylphenol, commonly known as thymol, is a naturally occurring compound found in plants such as thyme and oregano. It is a white crystalline substance with a pleasant, aromatic odor and possesses antiseptic and antifungal properties. Thymol is widely used in various applications due to its ability to destroy and inhibit the growth of microorganisms.
Uses
Used in Medicinal and Personal Care Products:
Thymol is used as an antiseptic and antifungal agent in medicinal and personal care products, such as mouthwashes, hand sanitizers, and topical antifungal creams. Its ability to destroy and inhibit the growth of microorganisms makes it an effective ingredient in these products.
Used in Food and Beverages:
Thymol is used as a flavoring agent in food and beverages, adding a unique taste and aroma to various products.
Used in Agriculture:
In the agricultural industry, thymol is used as a natural pesticide due to its ability to control and prevent the growth of harmful microorganisms and pests.
Used in Perfumes and Cosmetics Manufacturing:
Thymol is utilized in the manufacturing of perfumes and cosmetics for its pleasant aroma and as a preservative to maintain the freshness and longevity of the products.
Check Digit Verification of cas no
The CAS Registry Mumber 35050-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,5 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35050-88:
(7*3)+(6*5)+(5*0)+(4*5)+(3*0)+(2*8)+(1*8)=95
95 % 10 = 5
So 35050-88-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O/c1-4-9-6-8(3)7-10(5-2)11(9)12/h6-7,12H,4-5H2,1-3H3
35050-88-5Relevant articles and documents
Novel process for synthesizing high-steric-hindrance bromobenzene
-
Paragraph 0051-0056; 0065; 0066, (2019/01/23)
The invention relates to a novel process for synthesizing high-steric-hindrance bromobenzene. A preparing method of aryl bromide includes the steps of conducting reaction on aniline hydrobromide and inorganic nitrite in a two-phase or multi-phase system f
Three-component asymmetric catalytic ugi reaction - Concinnity from diversity by substrate-mediated catalyst assembly
Zhao, Wenjun,Huang, Li,Guan, Yong,Wulff, William D.
supporting information, p. 3436 - 3441 (2014/04/03)
The first chiral catalyst for the three-component Ugi reaction was identified as a result of a screen of a large set of different BOROX catalysts. The BOROX catalysts were assembled in situ from a chiral biaryl ligand, an amine, water, BH3×SMe2, and an alcohol or phenol. The catalyst screen included 13 different ligands, 12 amines, and 47 alcohols or phenols. The optimal catalyst system (LAP 8-5-47) provided α-amino amides from an aldehyde, a secondary amine, and an isonitrile with excellent asymmetric induction. The catalytically active species is proposed to be an ion pair that consists of the chiral boroxinate anion and an iminium cation. Harmonious arrangement of parts: A screen of BOROX catalysts that were generated in situ from 13 different ligands and 47 alcohols led to the identification of an effective combination for the catalytic asymmetric three-component Ugi reaction. Experimental results suggest that the catalyst is a chiral polyborate anion, which then forms an ion pair with the iminium cation that is generated from aldehyde and secondary amine.
