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2-(azepan-1-ylmethyl)-4,5-dimethylphenol is a complex organic compound with the molecular formula C16H23NO. It features a phenol group (a hydroxyl group attached to a benzene ring) with two methyl groups at the 4 and 5 positions, and an azepan-1-ylmethyl group attached to the 2 position. The azepan-1-ylmethyl group consists of a seven-membered azepan ring (a cyclic amine) with a methyl group attached to the nitrogen atom. 2-(azepan-1-ylmethyl)-4,5-dimethylphenol is known for its potential applications in the pharmaceutical and chemical industries, particularly as a building block for the synthesis of various drugs and other organic compounds. Its unique structure and properties make it an interesting target for research and development in the field of organic chemistry.

4969-29-3

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4969-29-3 Usage

Structure

A phenolic compound with a six-membered azepane ring attached to a methylated benzene ring

Usage

Commonly used in the pharmaceutical industry as a building block for the synthesis of various drug molecules

Potential properties

Has been studied for its potential anti-inflammatory and analgesic properties

Mechanism of action

Exact mechanism of action is still being investigated

Safety

Proper handling and storage procedures should be followed to ensure safety and prevent potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 4969-29-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,6 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4969-29:
(6*4)+(5*9)+(4*6)+(3*9)+(2*2)+(1*9)=133
133 % 10 = 3
So 4969-29-3 is a valid CAS Registry Number.

4969-29-3Upstream product

4969-29-3Downstream Products

4969-29-3Relevant academic research and scientific papers

Syntheses, analgetic activity, and physical dependence capacity of 5-phenyl-6,7-benzomorphan derivatives

Yokoyama,Almaula,Block,Granat,Gottfried,Hill,McMahon,Munch,Rachlin,Saelens,Siegel,Tomaselli,Clarke

, p. 537 - 553 (2007/10/04)

The synthesis, analgetic activity, and physical dependent capacity of a large number of 5-phenyl-6,7-benzomorphan derivatives are described. Observations made during the Stevens' rearrangement of 1-benzyl-1-methyl-Δ3-piperidinium salt derivatives (V) under various conditions are discussed. The absolute configuration of the 9-dimethyl series and the 2'-deoxy series is established by comparison of their ORD and CD spectra with those of ι-β-2'-hydroxy-2,9-dimethyl-5-phenyl-6,7-benzomorphan, whose absolute configuration was previously established by X-ray crystallography. A convenient synthesis of 3H-labeled phenols using 3H3PO4 is described, as well as the preparation of 14C-labeled compounds by conventional methods.

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