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28332-81-2

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28332-81-2 Usage

General Description

Acetamide, 2,2,2-trifluoro-N-(1-phenylethyl)- is a chemical compound with the molecular formula C11H11F3NO. It is a white solid substance that is commonly used as a building block or intermediate in organic synthesis. Acetamide, 2,2,2-trifluoro-N-(1-phenylethyl)- is notable for its trifluoromethyl group and phenylethyl substituents, which contribute to its unique chemical properties. Acetamide, 2,2,2-trifluoro-N-(1-phenylethyl)- is primarily utilized in the pharmaceutical and agrochemical industries for the synthesis of various biologically active compounds. Additionally, it has potential applications in research and development for the creation of new drugs or pesticides. Overall, this chemical compound plays a significant role in the production of diverse chemical products due to its versatile nature.

Check Digit Verification of cas no

The CAS Registry Mumber 28332-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,3 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28332-81:
(7*2)+(6*8)+(5*3)+(4*3)+(3*2)+(2*8)+(1*1)=112
112 % 10 = 2
So 28332-81-2 is a valid CAS Registry Number.

28332-81-2SDS

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 2,2,2-trifluoro-N-(1-phenylethyl)acetamide

1.2 Other means of identification

Product number -
Other names 2,2,2-trifluoro-N-((S)-1-phenylethyl)acetamide

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:28332-81-2 SDS

28332-81-2Relevant articles and documents

Tuning the Circular Dichroism and Circular Polarized Luminescence Intensities of Chiral 2D Hybrid Organic–Inorganic Perovskites through Halogenation of the Organic Ions

Chao, Yu-Chiang,Chen, Deng-Gao,Chiu, Ching-Wen,Chou, Pi-Tai,Lin, Jin-Tai,Lin, Tai-Chun,Liu, Yi-Hung,Yang, Lan-Sheng

supporting information, p. 21434 - 21440 (2021/08/20)

Through the incorporation of various halogen-substituted chiral organic cations, the effects of chiral molecules on the chiroptical properties of hybrid organic–inorganic perovskites (HOIPs) are investigated. Among them, the HOIP having a Cl-substituted chiral cation exhibits the highest circular dichroism (CD) and circular polarized luminescence (CPL) intensities, indicating the existence of the largest rotatory strength, whereas the F-substituted HIOP shows the weakest intensities. The observed modulation can be correlated to the varied magnetic transition dipole of HOIPs, which is sensitive to the d-spacing between inorganic layers and the halogen–halogen interaction between organic cations and the inorganic sheets. These counteracting effects meet the optimal CD and CPL intensity with chlorine substitution, rendering the rotatory strength of HOIPs arranged in the order of (ClMBA)2PbI4>(BrMBA)2PbI4>(IMBA)2PbI4>(MBA)2PbI4>(FMBA)2PbI4.

Diastereoselective synthesis of polyfluoroalkylated α-aminophosphonic acid derivatives

Stanko, Oleg V.,Rassukana, Yuliya V.,Zamulko, Kateryna A.,Dyakonenko, Viktoriya V.,Shishkina, Svitlana V.,Onys'ko, Petro P.

, p. 47 - 56 (2018/10/21)

The asymmetric synthesis of biorelevant aminophosphonates and aminophosphonic acids bearing trifluoromethyl, tetrafluoroethyl, perfluoropropyl or chlorodifluoromethyl group in the α-position to phosphonyl group is developed. Diastereoselective reduction o

Acetic acid as a catalyst for the N-acylation of amines using esters as the acyl source

Sanz Sharley, Daniel D.,Williams, Jonathan M. J.

supporting information, p. 2020 - 2023 (2017/02/15)

We report a cheap and simple method for the acetylation of a variety of amines using catalytic acetic acid and either ethyl acetate or butyl acetate as the acyl source. Catalyst loadings as low as 10 mol% afforded acetamide products in excellent yields at temperatures ranging from 80-120 °C. The methodology can also be successfully applied for the synthesis of a broad range of other amides, including the formation of formamides at 20 °C.

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