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1-Butanone, 1-[4-(trifluoromethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37851-10-8

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37851-10-8 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

This is the widely recognized name for the compound, which is derived from its structure and properties.

Explanation

The compound exists in a liquid state at room temperature and is colorless in appearance.

Explanation

The compound has a noticeable and intense smell.

Explanation

The compound can dissolve in organic solvents, making it useful for various applications in the chemical industry.

Explanation

The compound is used as a solvent in the production of pharmaceuticals, as well as in the creation of fragrances and flavors due to its solubility and chemical properties.

Explanation

The compound serves as a building block or reagent in the creation of other organic compounds, contributing to its importance in the chemical industry.

Explanation

The compound is utilized in chemical reactions to facilitate or catalyze specific transformations, making it a valuable tool in the laboratory.

Explanation

Due to its potential hazards, it is crucial to handle and store the compound with care to prevent accidents or health risks.

Explanation

The compound's structure consists of a butanone group (a four-carbon chain with a carbonyl group at the end) and a 4-(trifluoromethyl)phenyl group (a phenyl ring with a trifluoromethyl group attached to the fourth carbon).

Physical State

Colorless liquid

Odor

Strong

Solubility

Soluble in organic solvents

Industrial Applications

a. Solvent in pharmaceutical production
b. Manufacturing of fragrances and flavors

Chemical Synthesis

Used in the synthesis of various organic compounds

Chemical Reactions

Used as a reagent

Hazardous Nature

Requires proper handling and storage

Chemical Structure

Contains a butanone group and a 4-(trifluoromethyl)phenyl group

Check Digit Verification of cas no

The CAS Registry Mumber 37851-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,8,5 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37851-10:
(7*3)+(6*7)+(5*8)+(4*5)+(3*1)+(2*1)+(1*0)=128
128 % 10 = 8
So 37851-10-8 is a valid CAS Registry Number.

37851-10-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-(trifluoromethyl)phenyl]butan-1-one

1.2 Other means of identification

Product number -
Other names 1-Butanone,1-[4-(trifluoromethyl)phenyl]

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:37851-10-8 SDS

37851-10-8Relevant academic research and scientific papers

CARBAMATE DERIVATIVES AND USES THEREOF

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Paragraph 01419-01420, (2020/08/13)

The present disclosure relates to compounds of Formula (I): and to their prodrugs, pharmaceutically acceptable salts, pharmaceutical compositions, methods of use, and methods for their preparation. The compounds disclosed herein are useful for inhibiting the maturation of cytokines of the IL-1 family by inhibiting inflammasomes and may be used in the treatment of disorders in which inflammasome activity is implicated, such as inflammatory, autoinflammatory and autoimmune diseases and cancers.

Acylation of aryl halides and α-bromo acetates with aldehydes enabled by nickel/tbadt cocatalysis

Fan, Pei,Zhang, Chang,Zhang, Linchuan,Wang, Chuan

supporting information, p. 3875 - 3878 (2020/05/14)

In this protocol aryl halides and α-bromo acetates are efficiently cross-coupled with an array of (hetero)aromatic and aliphatic aldehydes under the cooperative catalysis of nickel and tetrabutylammonium decatungstate as a hydrogen-atom-transfer photocatalyst. This method provides a concise approach to a variety of ketones with high compatibility of various functional groups.

Dirhodium(ii)/P(t-Bu)3 catalyzed tandem reaction of α,β-unsaturated aldehydes with arylboronic acids

Ma, Ziling,Wang, Yuanhua

supporting information, p. 7470 - 7476 (2018/10/24)

Phosphine ligated dirhodium(ii) acetate is advocated as a catalyst for the synthesis of aryl alkyl ketones by the tandem reaction of α,β-unsaturated aromatic or aliphatic aldehydes with arylboronic acids. This tandem procedure included arylation followed by the isomerization reaction. This method exhibits good functional group tolerance and has a broad substrate scope. With the conjugated aldehydes, the one-step synthesis of γ,δ-unsaturated ketones was realized through this reaction. It is noteworthy that the length of the Rh-P bond is an important factor affecting catalytic reactions. The comparative analysis of the crystal structures of axially alkylphosphane and arylphosphane ligated dirhodium(ii) acetate revealed that the shorter Rh-P bond length favors the isomerization process as compared to the longer one. In addition, the dirhodium(ii) compound can be recovered after the completion of the reaction.

Photocatalytic E → Z isomerization of polarized alkenes inspired by the visual cycle: Mechanistic dichotomy and origin of selectivity

Metternich, Jan B.,Artiukhin, Denis G.,Holland, Mareike C.,Von Bremen-Kuhne, Maximilian,Neugebauer, Johannes,Gilmour, Ryan

, p. 9955 - 9977 (2018/05/31)

Iteratively executed with exquisite spatial and temporal control, the selective isomerization of polarized alkenes underpins a plethora of complex biological processes ranging from natural product biosynthesis through to the mammalian visual cycle. However, nature's proficiency conceals the inherent difficulties in replicating this contrathermodynamic transformation in the laboratory. Recently, we disclosed the first highly Z-selective isomerization of polarized alkenes, employing the cinnamoyl chromophore as a retinal surrogate under UV-irradiation (402 nm) with (-)-riboflavin (Vitamin B2) as an inexpensive, organic photocatalyst (J. Am. Chem. Soc. 2015, 137, 11254-11257). This study was inspired by the propensity of crystalline (-)-riboflavin in the eyes of vertebrates to invert the intrinsic directionality of retinal isomerization. Herein, we extend this methodology to include a bioinspired, catalytic E → Z isomerization of α,β-unsaturated nitriles, thereby mimicking the intermediate Opsin-derived, protonated Schiff base in the visual cycle with simple polarized alkenes. Replacement of the iminium motif by a cyano group is well tolerated and gives an additional degree of versatility for postisomerization functionalization. Broad substrate scope is demonstrated (up to 99:1 Z:E) together with evidence of mechanistic dichotomy via both singlet and triplet energy transfer mechanisms. Kinetic studies, temperature dependent photostationary state correlations and investigation of substituent-based electronic perturbation of the alkene identified polarization combined with increased Z-isomer activation barriers as the selectivity governing factors in catalysis. This investigation demonstrates the importance of internal structural preorganization on photostationary composition and explicates the augmented Z-selectivity upon hydrogen-alkyl exchange at the β-position of the alkene.

Palladium-catalyzed synthesis of aryl ketones by coupling of aryl bromides with an acyl anion equivalent

Takemiya, Akihiro,Hartwig, John F.

, p. 14800 - 14801 (2008/02/05)

Palladium-catalyzed couplings of aryl bromides with N-tert-butylhydrazones as acyl anion equivalents to form aryl ketones are reported. The coupling process occurs at the C-position of hydrazones to form N-tert-butyl azo compounds. Isomerization of these azo compounds to the corresponding hydrazones, followed by hydrolysis, gave the desired mixed alkyl aryl ketones. The selectivity of C- versus N-arylation was strongly influenced by the substituent on nitrogen. Arylation at carbon occurred with N-tert-butylhydrazones, whereas N-arylation occurred with N-arylhydrazones. The arylation of hydrazones containing primary and secondary alkyl groups, as well as aryl groups, gave the desired ketones in good yields after hydrolysis. Functional groups on the aromatic ring, such as alkoxy, cyano, trifluoromethyl, carboalkoxy, carbamoyl, and keto groups, were tolerated. This reaction likely occurs by C-C bond-forming reductive elimination from an intermediate containing an η1-diazaallyl ligand. Copyright

TREATMENT FOR ALZHEIMER'S DISEASE AND RELATED CONDITIONS

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Page/Page column 55, (2010/02/10)

Compounds of formula (I): are useful in the treatment of diseases associated with deposition of β-amyloid in the brain.

Direct catalytic asymmetric aldol-Tishchenko reaction

Gnanadesikan, Vijay,Horiuchi, Yoshihiro,Ohshima, Takashi,Shibasaki, Masakatsu

, p. 7782 - 7783 (2007/10/03)

A direct catalytic asymmetric aldol reaction of propionate equivalent was achieved via the aldol-Tishchenko reaction. Coupling an irreversible Tishchenko reaction to a reversible aldol reaction overcame the retro-aldol reaction problem and thereby afforde

Derivatives of an aminoketone

-

, (2008/06/13)

A new class of aminoketone derivatives according to the formula: STR1 and certain propiophenone derivatives in particular, corresponding to the formula: STR2 having central muscle relaxant activity.

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