439108-60-8

Basic information

• Product Name: (5-PHENYL-2-THIENYL)METHANOL
• Synonyms: RARECHEM AL BD 0489;(5-PHENYL-2-THIENYL)METHANOL;(5-phenylthiophen-2-yl)methanol
• CAS NO: 439108-60-8
• Molecular Formula: C₁₁H₁₀OS
• Molecular Weight: 190.26
• Mol File: 439108-60-8.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (5-PHENYL-2-THIENYL)METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (5-PHENYL-2-THIENYL)METHANOL(439108-60-8)
• EPA Substance Registry System: (5-PHENYL-2-THIENYL)METHANOL(439108-60-8)

Safety Data

• Hazardous Substances Data: 439108-60-8(Hazardous Substances Data)

Usage

Description

(5-PHENYL-2-THIENYL)METHANOL, with the molecular formula C12H10OS, is a white solid chemical compound at room temperature. It features a phenyl group and a thienyl group, making it a versatile building block for the synthesis of complex organic molecules. (5-PHENYL-2-THIENYL)METHANOL is also recognized for its potential biological activity, as it has been studied for its antifungal and antiviral properties. Furthermore, it serves as a reagent in organic synthesis reactions, allowing the introduction of the (5-phenyl-2-thienyl)methanol functional group into various compounds. (5-PHENYL-2-THIENYL)METHANOL is a valuable chemical with a broad spectrum of applications in the fields of chemistry and pharmaceuticals.

Uses

Used in Chemical Synthesis:
(5-PHENYL-2-THIENYL)METHANOL is used as a versatile building block for the synthesis of complex organic molecules due to its phenyl and thienyl groups.
Used in Pharmaceutical Applications:
(5-PHENYL-2-THIENYL)METHANOL is used as a compound with potential biological activity, particularly for its antifungal and antiviral properties.
Used in Organic Synthesis Reactions:
(5-PHENYL-2-THIENYL)METHANOL is used as a reagent to introduce the (5-phenyl-2-thienyl)methanol functional group into various compounds, enhancing their properties and applications.

Upstream product

• 19163-24-7 5-phenyl-2-thiophenecarboxylic acid 
• 825-55-8 2-phenylthiophene 
• 98-80-6 phenylboronic acid 
• 19163-21-4 5-phenylthiophene-2-carboxaldehyde 
• 4701-17-1 5-bromo-2-thiophencarboxaldehyde 
• 19282-39-4 ethyl 5-phenylthiophene-2-carboxylate 
• 33603-87-1 (Z)-3-chloro-3-phenyl-2-propenal 
• 98-86-2 acetophenone 

Downstream Products

• 19163-21-4 5-phenylthiophene-2-carboxaldehyde 
• 1255762-86-7 1-(5-phenylthiophen-2-ylmethyl)-1H-imidazole 
• 825-55-8 2-phenylthiophene 
• 1361312-11-9 2-(2-methyl-2-propenyloxy)methyl-5-phenylthiophene 
• 1361312-06-2 2-(3-methyl-2-butenyloxy)methyl-5-phenylthiophene 
• 1361312-12-0 2-phenyl-5-(2-propenyloxy)methylthiophene 
• 1361312-09-5 2-(2,3-dimethyl-2-butenyloxy)methyl-5-phenylthiophene 
• 1361312-10-8 2-[(E)-2-methyl-2-butenyloxy]methyl-5-phenylthiophene 
• 147380-63-0 N-hydroxy-N-[2-(5-phenylthien-2-ylmethoxy)ethyl] urea 

Relevant articles and documents

Metal-Free Aerobic Oxidative Selective C-C Bond Cleavage in Heteroaryl-Containing Primary and Secondary Alcohols

A transition-metal-free aerobic oxidative selective C-C bond-cleavage reaction in primary and secondary heteroaryl alcohols is reported. This reaction was highly efficient and tolerated various heteroaryl alcohols, generating a carboxylic acid derivative and a neutral heteroaromatic compound. Experimental studies combined with density functional theory calculations revealed the mechanism underlying the selective C-C bond cleavage. This strategy also provides an alternative simple approach to carboxylation reaction.

Oxazolidinone compound containing piperazine hydrazone structure

The invention discloses an oxazolidinone compound containing a piperazine hydrazone structure. The oxazolidinone compound comprises a compound shown as a general formula (I), or stereisomer thereof, or pharmaceutically-acceptable salt thereof, or solvate thereof or prodrug thereof, wherein R1 is hydrogen, fluorine, chlorine or trifluoromethyl, R2 is -NHCOCH3 or -OH, R3 is Ar which is C5-C10 aryl substituted by any 1-3 R4 and heteroaryl, and R4 is hydrogen, hydroxyl, halogen, nitro, amino, cyan, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 alkyl substituted by hydroxyl, amino or halogen, C1-C6 alkoxy substituted by hydroxyl, amino or halogen, amino substituted by mono- or bi-(C1-C6 alkyl), C1-C6 alkyl amido, free, salty, esterified and amidated hydroxyl, C1-C6 alkyl sulfinyl, C1-C6 alkyl sulfonyl, C1-C6 alkyl acyl and carbamoyl. The oxazolidinone compound can be used for preparing drug for treating microbial infection.

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