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186203-15-6

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186203-15-6 Usage

Description

(1-Benzyl-3-trifluoromethyl-pyrrolidin-3-yl)-methanol is a complex chemical compound with potential pharmaceutical applications. It features a benzyl group, a trifluoromethyl group, and a pyrrolidin-3-yl group, all connected to a central methanol moiety. The presence of the pyrrolidin-3-yl group, a common structural element in psychoactive substances, suggests that this compound may have effects on the central nervous system. Additionally, the trifluoromethyl group imparts unique chemical and biological properties to the molecule. (1-Benzyl-3-trifluoromethyl-pyrrolidin-3-yl)-methanol's diverse structure indicates a broad range of potential applications in medicine and pharmacology, although further research is necessary to fully explore its properties and uses.

Uses

Used in Pharmaceutical Industry:
(1-Benzyl-3-trifluoromethyl-pyrrolidin-3-yl)-methanol is used as a potential active pharmaceutical ingredient for its possible effects on the central nervous system due to the presence of the pyrrolidin-3-yl group. Its unique structure and the properties conferred by the trifluoromethyl group make it a candidate for the development of new medications, particularly those targeting the central nervous system.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (1-Benzyl-3-trifluoromethyl-pyrrolidin-3-yl)-methanol serves as a valuable compound for studying the structure-activity relationships of psychoactive substances. Its diverse functional groups provide a basis for exploring how modifications to the molecule can influence its biological activity and potential therapeutic effects.
Used in Drug Design and Development:
(1-Benzyl-3-trifluoromethyl-pyrrolidin-3-yl)-methanol is utilized in drug design and development processes to create novel therapeutic agents. Its unique combination of functional groups offers opportunities for the design of drugs with specific targeting and action mechanisms, potentially leading to more effective treatments for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 186203-15-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,2,0 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 186203-15:
(8*1)+(7*8)+(6*6)+(5*2)+(4*0)+(3*3)+(2*1)+(1*5)=126
126 % 10 = 6
So 186203-15-6 is a valid CAS Registry Number.

186203-15-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-benzyl-3-(trifluoromethyl)pyrrolidin-3-yl]methanol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:186203-15-6 SDS

186203-15-6Relevant articles and documents

ALKYNYL QUINAZOLINE COMPOUNDS

-

, (2021/02/19)

The present disclosure relates to compounds of Formula (I'): and pharmaceutically acceptable salts and stereoisomers thereof. The present disclosure also relates to methods of preparation these compounds, compositions comprising these compounds, and methods of using them in the prevention or treatment of abnormal cell growth in mammals, especially humans.

Synthesis and antibacterial activity of novel 7-(3-substituted-3 or 4- trifluoromethyl-1-pyrrolidinyl)-8-methoxyfluoroquinolones

Fukui, Hideto,Shibata, Tetsuo,Naito, Takanobu,Nakano, Jun,Maejima, Tetsuro,Senda, Hisato,Iwatani, Wakao,Tatsumi, Yoshiyuki,Suda, Masahiro,Arika, Tadashi

, p. 2833 - 2838 (2007/10/03)

The titled compounds were synthesized and evaluated for in vitro antibacterial activity. The (3R,4S)3-aminomethyl-4-trifluoromethyl derivative (S-34109) was confirmed to be optimal because of its superior activity against quinolone and methicillin-resistant Staphyrococcus aureus and low side effect potential.

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