464920-07-8 Usage
Derivative of
1,3-Benzenediol (resorcinol)
Structural feature
Presence of a butyl group with two hydroxyl groups attached to a benzene ring
Natural sources
Found in fruits, vegetables, and certain essential oils
Properties
a. Antioxidant
b. Antibacterial
Potential applications
a. Cosmetic industry
b. Pharmaceutical industry
c. Synthesis of novel biologically active compounds
These properties and contents provide a comprehensive overview of 1,3-Benzenediol, 4-(2,3-dihydroxy-3-methylbutyl)(9CI), highlighting its chemical structure, natural occurrence, and potential uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 464920-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,4,9,2 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 464920-07:
(8*4)+(7*6)+(6*4)+(5*9)+(4*2)+(3*0)+(2*0)+(1*7)=158
158 % 10 = 8
So 464920-07-8 is a valid CAS Registry Number.
464920-07-8Relevant articles and documents
Synthesis of the F11334's from o-prenylated phenols: ΜM inhibitors of neutral sphingomyelinase (N-SMase)
Lindsey, Christopher C,Gómez-Díaz, Consuelo,Villalba, José M,Pettus, Thomas R.R
, p. 4559 - 4565 (2002)
F11334A1, F11334A2, F11334A3, and their corresponding resorcinol analogs were synthesized along with F11334B1, and F11263. In the course of these synthetic studies, several conditions for manipulating (2,3-propanediol) and (2,3-epoxypropyl) o-substituted phenols were developed as well as a variety of conditions for cleavage of aryl O-t-butyl carbonates. From enzyme assays it appears that the hydroquinone nucleus is the essential structural necessary for N-SMase inhibition. Furthermore, it appears that this family of compounds is comprised of irreversible inhibitors.
