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2-(Trifluoromethyl)benzhydrol, with the chemical formula C8H7F3O, is a white solid chemical compound that exhibits solubility in organic solvents but not in water. It is recognized for its high reactivity, making it a valuable building block in the synthesis of pharmaceuticals and other organic compounds. Its potential as an intermediate in the production of a diverse range of chemical compounds is notable. Moreover, it has demonstrated antibacterial properties and is under investigation for its possible applications in medicine, highlighting its versatility in both the pharmaceutical and chemical industries.

727-98-0

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727-98-0 Usage

Uses

Used in Pharmaceutical Synthesis:
2-(Trifluoromethyl)benzhydrol is utilized as a key building block in the creation of various pharmaceuticals due to its high reactivity, which allows for the development of a wide array of chemical compounds with potential therapeutic applications.
Used in Organic Compounds Synthesis:
In the realm of organic chemistry, 2-(trifluoromethyl)benzhydrol serves as an essential component in the synthesis of numerous organic compounds, contributing to the structural diversity and functional properties of these molecules.
Used in Antibacterial Agents Development:
Leveraging its inherent antibacterial properties, 2-(trifluoromethyl)benzhydrol is being explored for its potential as a component in new antibacterial agents, which could be crucial in addressing the growing challenge of antibiotic resistance.
Used in Chemical Industry:
Beyond its pharmaceutical applications, 2-(trifluoromethyl)benzhydrol is also recognized for its utility in the broader chemical industry, where it can be employed as an intermediate in the production of a variety of chemical compounds for different uses.

Check Digit Verification of cas no

The CAS Registry Mumber 727-98-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 727-98:
(5*7)+(4*2)+(3*7)+(2*9)+(1*8)=90
90 % 10 = 0
So 727-98-0 is a valid CAS Registry Number.

727-98-0SDS

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 2-(Trifluoromethyl)benzhydrol

1.2 Other means of identification

Product number -
Other names phenyl-[2-(trifluoromethyl)phenyl]methanol

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:727-98-0 SDS

727-98-0Relevant academic research and scientific papers

Chiral electron-rich PNP ligand with a phospholane motif: Structural features and application in asymmetric hydrogenation

Wang, Heng,Zhang, Yao,Yang, Tilong,Guo, Xiaochong,Gong, Quan,Wen, Jialin,Zhang, Xumu

supporting information, p. 8796 - 8801 (2020/11/13)

Despite the remarkable reactivity that was achieved by a series of transition-metal catalysts with a PNP type ligand, the electron-rich chiral PNP ligands have still been rarely reported because of the difficulties in synthesis and the nature of air-sensitivity. Herein, we report a novel chiral PNP ligand (Heng-PNP) with both a rigid backbone and a bulky tert-butyl group on the phospholane motif. We successfully obtained its divalent iron complex. The chiral environment of its Ir(III) complex was also discussed with quadrant analysis. This tridentate ligand was applied in iridium-catalyzed asymmetric hydrogenation of challenging diaryl ketones: up to 98% ee and 500 TON are achieved. Computational study showed that the twist of conjugate aryl group in the substrate (induced by the special chiral pocket of Ir/Heng-PNP complex) leads to the energy difference in the enantiodetermining step.

NMO·TPB: A selectivity variation on the Ley-Griffith TPAP oxidation

Moore, Peter W.,Mirzayans, Paul M.,Williams, Craig M.

supporting information, p. 3567 - 3571 (2015/03/04)

A non-hygroscopic tetraphenylborate salt of N-methylmorpholine-N-oxide (NMO) is reported (NMO·TPB), which modulates the standard Ley-Griffith oxidation such that benzylic and allylic alcohols are oxidised selectively. An attractive feature of this new protocol is that anhydrous conditions are not required for this selective tetra-n-propylammonium perruthenate (TPAP) oxidation, superseding the requirement of molecular sieves.

From in vitro to in cellulo: Structure-activity relationship of (2-nitrophenyl)methanol derivatives as inhibitors of PqsD in Pseudomonas aeruginosa

Storz, Michael P.,Allegretta, Giuseppe,Kirsch, Benjamin,Empting, Martin,Hartmann, Rolf W.

supporting information, p. 6094 - 6104 (2014/08/05)

Recent studies have shown that compounds based on a (2-nitrophenyl)methanol scaffold are promising inhibitors of PqsD, a key enzyme of signal molecule biosynthesis in the cell-to-cell communication of Pseudomonas aeruginosa. The most promising molecule displayed anti-biofilm activity and a tight-binding mode of action. Herein, we report on the convenient synthesis and biochemical evaluation of a comprehensive series of (2-nitrophenyl)methanol derivatives. The in vitro potency of these inhibitors against recombinant PqsD as well as the effect of selected compounds on the production of the signal molecules HHQ and PQS in P. aeruginosa were examined. The gathered data allowed the establishment of a structure-activity relationship, which was used to design fluorescent inhibitors, and finally, led to the discovery of (2-nitrophenyl)methanol derivatives with improved in cellulo efficacy providing new perspectives towards the application of PqsD inhibitors as anti-infectives. This journal is the Partner Organisations 2014.

Bu4N+ alkoxide-initiated/autocatalytic addition reactions with organotrimethylsilanes

Das, Manas,O'Shea, Donal F.

, p. 5595 - 5607 (2014/07/08)

The use of Me3SiO-/Bu4N+ as a general activator of organotrimethylsilanes for addition reactions has been established. The broad scope of the method offers trimethylsilanes (including acetate, allyl, propargyl, benzyl, dithiane, heteroaryl, and aryl derivatives) as bench-stable organometallics that can be readily utilized as carbanion equivalents for synthesis. Reactions are achieved at rt without the requirement of specialized precautions that are commonplace for other organometallics.

Structure-activity relationships of diphenylpiperazine N-type calcium channel inhibitors

Pajouhesh, Hassan,Feng, Zhong-Ping,Ding, Yanbing,Zhang, Lingyun,Pajouhesh, Hossein,Morrison, Jerrie-Lynn,Belardetti, Francesco,Tringham, Elizabeth,Simonson, Eric,Vanderah, Todd W.,Porreca, Frank,Zamponi, Gerald W.,Mitscher, Lester A.,Snutch, Terrance P.

scheme or table, p. 1378 - 1383 (2010/07/06)

A novel series of compounds derived from the previously reported N-type calcium channel blocker NP118809 (1-(4-benzhydrylpiperazin-1-yl)-3,3-diphenylpropan-1-one) is described. Extensive SAR studies resulted in compounds with IC50 values in the range of 10-150 nM and selectivity over the L-type channels up to nearly 1200-fold. Orally administered compounds 5 and 21 exhibited both anti-allodynic and anti-hyperalgesic activity in the spinal nerve ligation model of neuropathic pain.

Highly efficient and facile aryl transfer to aldehydes using ArB(OH) 2-GaMe3

Jia, Xuefeng,Fang, Ling,Lin, Aijun,Pan, Yi,Zhu, Chengjian

body text, p. 495 - 499 (2009/09/08)

A rapid and efficient procedure for the synthesis of diarylmethanols has successfully been achieved by the aryl transfer to aldehydes using the ArB(OH)2-GaMe3 combined systems in excellent yields (up to 98%) at room temperature. Georg Thieme Verlag Stuttgart.

Microwave irradiation as a high-speed tool for activation of sluggish aryl chlorides in Grignard reactions

Gold, Henrik,Larhed, Mats,Nilsson, Peter

, p. 1596 - 1600 (2007/10/03)

Grignard reagents have been generated from reluctant aryl chlorides and bromides using controlled microwave heating to establish a safe, productive and reproducible method. In the synthesis of a novel HIV-1 protease inhibitor, microwave irradiation was both used to generate the starting arylmagnesium halide and to promote a subsequent Kumada coupling. Georg Thieme Verlag Stuttgart.

AZETIDINECARBOXAMIDE DERIVATIVES AND THEIR USE IN THE TREATMENT OF CB1 RECEPTOR MEDIATED DISORDERS

-

Page 62, (2008/06/13)

Compounds of formula (I) and their use in therapy, particularly for the treatment of a disorder mediated by CB1 receptors such as obesity: Formuila (I) wherein: R1 and R2 are independently selected from aryl; and R3 is hydrogen or alkyl; or a pharmaceutically acceptable salt or prodrug thereof, wherein at least one of R1 and R2 has a non-hydrogen substituent in the ortho-position(s) thereof relative to the point of attachment to the [-CH-0-] group.

Preparation of organomanganese reagents from organic halides with activated manganese

Kakiya, Hirotada,Nishimae, Shinji,Shinokubo, Hiroshi,Oshima, Koichiro

, p. 8807 - 8815 (2007/10/03)

Reduction of Li2MnCl4 with magnesium metal provided activated manganese as a black suspension in THF. Treatment of organic halides such as allyl bromides, α-halo esters or aryl halides with activated manganese furnished various organomanganese reagents which reacted further with electrophiles to afford the corresponding adducts. The reaction of a ketone bearing an iodoaryl moiety with this active manganese induced cyclization to provide dihydroindene derivative.

Preparation of allyl-, alkenyl- and of functionalized arylmanganese reagents by oxidative insertion of manganese-graphite into organic halides

Fuerstner, Alois,Brunner, Heiko

, p. 7009 - 7012 (2007/10/03)

Reduction of MnBr2·nLiBr (n = 1,2) with 2 C8K in THF affords highly active Mn-graphite, which readily insert into allyl-, alkenyl-, (substituted) aryl- and heteroaryl halides. The functionalized organomanganese compounds thus obtained may be efficiently trapped with different electrophiles such as aldehydes, anhydrides and acid chlorides, or can be cross-coupled with alkenyl halides in the presence of catalytic amounts of Fe(acac)3.

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