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(4-(Adamantan-1-yl)phenyl)methanol is a complex organic compound with the molecular formula C18H22O. It is characterized by a phenyl group (a benzene ring) connected to an adamantane moiety, which is a rigid, cage-like structure consisting of four fused cyclohexane rings. The hydroxyl group (-OH) is attached to the benzylic carbon, making it a primary alcohol. (4-(adamantan-1-yl)phenyl)methanol is known for its unique stereochemistry and potential applications in the synthesis of pharmaceuticals and other organic compounds due to its rigid structure and ability to form stable derivatives. It is typically synthesized through various chemical reactions and can be used as a building block in the creation of more complex molecules.

7131-08-0

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7131-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7131-08-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,3 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7131-08:
(6*7)+(5*1)+(4*3)+(3*1)+(2*0)+(1*8)=70
70 % 10 = 0
So 7131-08-0 is a valid CAS Registry Number.

7131-08-0Relevant academic research and scientific papers

Alkylation of aromatic compounds with 1-bromoadamantane in the presence of metal complex catalysts

Khusnutdinov,Shchadneva,Khisamova

, p. 1545 - 1550 (2015/12/30)

Synthesis of aryladamantanes was performed by reaction of 1-bromoadamantane with aromatic compounds in the presence of metal complex catalysts containing Mo, Cr, W, Cu, and Co.

CARBAMATE DERIVATIVES OF LACTAM BASED N-ACYLETHANOLAMINE ACID AMIDASE (NAAA) INHIBITORS

-

, (2014/09/29)

Described herein are compounds and pharmaceutical compositions which inhibit N-acylethanolamine acid amidase (NAAA). Described herein are methods for synthesizing the compounds set forth herein and methods for formulating these compounds as pharmaceutical compositions which include these compounds. Also described herein are methods of inhibiting NAAA in order to sustain the levels of palmitoylethanolamide (PEA) and other N-acylethanolamines (NAE) that are substrates for NAAA, in conditions characterized by reduced concentrations of NAE. Also, described here are methods of treating and ameliorating pain, inflammation, inflammatory diseases, and other disorders in which modulation of fatty acid ethanolamides is clinically or therapeutically relevant or in which decreased levels of NAE are associated with the disorder.

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