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4-iodobenzhydrol, also known as 4-iododiphenylmethanol or 4-iodobenzhydryl alcohol, is an organic compound with the chemical formula C13H11IO. It is a colorless to pale yellow crystalline solid that is soluble in organic solvents such as ethanol, acetone, and dichloromethane. 4-iodobenzhydrol is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. 4-iodobenzhydrol is obtained through the iodination of benzhydrol, a process that involves the reaction of benzhydrol with iodine and a suitable catalyst, such as iodine monobromide or iodine monochloride. Due to its reactivity and the presence of the iodine atom, it can be further functionalized or used in cross-coupling reactions to form a variety of complex molecules.

172483-72-6

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172483-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 172483-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,4,8 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 172483-72:
(8*1)+(7*7)+(6*2)+(5*4)+(4*8)+(3*3)+(2*7)+(1*2)=146
146 % 10 = 6
So 172483-72-6 is a valid CAS Registry Number.

172483-72-6Relevant academic research and scientific papers

Compounds for Treating Cannabinoid Toxicity and Acute Cannabinoid Overdose

-

, (2022/02/11)

The present invention relates to novel compounds that can act as antidotes for treating “Acute Cannabinoid Overdose” produced by classical cannabinoids such as Δ9-tetrahydrocannabinol (THC) and several synthetic psychoactive cannabinoids (SPCs). The cannabis constituent THC exerts its psychotropic effects via CB1 receptor activation and SPCs mimic the effects of THC with higher potency and severe neurotoxicity. Compounds disclosed in this invention, their enantiomers, diastereomers, geometric isomers, racemates, tautomers, rotamers, atropisomers, metabolites, N-oxides, salts, solvates, hydrates, isotopic variations and their polymorphic forms can be therapeutically useful in an emergency setting for counteracting the intoxicating effects of acute THC ingestion and SPC overdose. Also, aspects of the invention are concerned with pyrazoles, imidazoles, triazoles, thiazoles, oxazoles, dihydropyrazoles, pyrrolidinones, azetidines, oxyazetidines and azaspiro[3.3]heptanes with unique pharmacokinetic and pharmacodynamic properties for treating “Acute Cannabinoid Overdose”.

Hypophosphorous acid-iodine: A novel reducing system. Part 2: Reduction of benzhydrols to diarylmethylene derivatives

Gordon, Paul E.,Fry, Albert J.

, p. 831 - 833 (2007/10/03)

A mixture of hypophosphorous acid (H3PO2) and iodine in acetic acid reduces a variety of substituted benzhydrols to the corresponding methylene derivatives in very high yields. The active reducing agent is hydrogen iodide generated by reaction between iodine and hypophosphorous acid.

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