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464920-07-8

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464920-07-8 Usage

General Description

1,3-Benzenediol, 4-(2,3-dihydroxy-3-methylbutyl)- (9CI), also known as 2,3-dihydroxy-3-methylbutyl-4-hydroxyphenyl, is a chemical compound with the molecular formula C11H16O4. It is a derivative of 1,3-Benzenediol, also known as resorcinol, and is characterized by the presence of a butyl group with two hydroxyl groups attached to a benzene ring. This chemical is commonly found in a variety of natural sources, including fruits, vegetables, and certain essential oils. It has antioxidant and antibacterial properties, making it potentially useful for cosmetic and pharmaceutical applications. Additionally, it has been studied for its potential role in the synthesis of novel biologically active compounds. Overall, 1,3-Benzenediol, 4-(2,3-dihydroxy-3-methylbutyl)- (9CI) is a versatile compound with various potential applications in different fields.

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.

464920-07-8Downstream Products

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.

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