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31165-67-0

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31165-67-0 Usage

General Description

2'-BENZYLOXYACETOPHENONE is a chemical compound with the molecular formula C15H14O2. It is a white to off-white crystalline powder that is commonly used in the synthesis of various pharmaceutical compounds and organic materials. 2'-BENZYLOXYACETOPHENONE is known for its aromatic and benzyl properties, making it useful in the production of fragrances, flavorings, and other aromatic products. Additionally, 2'-BENZYLOXYACETOPHENONE has potential applications in the field of organic synthesis and medicinal chemistry, as it can be utilized in the preparation of various biologically active molecules. Overall, this chemical plays a crucial role in the development of pharmaceuticals and organic compounds, and its versatile properties make it a valuable component in chemical research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 31165-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,6 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 31165-67:
(7*3)+(6*1)+(5*1)+(4*6)+(3*5)+(2*6)+(1*7)=90
90 % 10 = 0
So 31165-67-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O2/c1-12(16)14-9-5-6-10-15(14)17-11-13-7-3-2-4-8-13/h2-10H,11H2,1H3

31165-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2'-Benzyloxyacetophenone

1.2 Other means of identification

Product number -
Other names 1-(2-phenylmethoxyphenyl)ethanone

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:31165-67-0 SDS

31165-67-0Relevant articles and documents

Conformational analysis: 3JHCOC and 3JHCCC Karplus relationships for methylene 1H nuclei

Grimmer, Craig D.,Slabber, Cathryn A.

, p. 590 - 595 (2015)

NAMFIS (NMR Analysis of Molecular Flexibility In Solution) was applied to 1-[2-(benzyloxy)phenyl]ethanone using quantitative 1H-1H NOE distances and 3J proton-carbon coupling constant (CC) restraints for averaged methylene

Method for synthesizing aryl benzyl ether compound

-

Paragraph 0027; 0041, (2021/04/14)

The invention discloses a method for synthesizing aryl benzyl ether compounds, which comprises the following steps: by using an iron (III) complex containing 1, 3-di-tert-butyl imidazole cations and having a molecular formula of [(tBuNCH = CHNtBu) CH] [FeBr4] as a catalyst and di-tert-butyl peroxide as an oxidant, carrying out oxidative coupling reaction on phenolic compounds and toluene compounds to synthesize the corresponding aryl benzyl ether compounds. The method is the first example for preparing the aryl benzyl ether compound through the oxidative coupling reaction of the phenolic compound and the toluene compound, which is realized by an iron-based catalyst, and has the advantages of atom economy, environmental friendliness and good substrate applicability.

Design, synthesis and biological activity of selective hCAs inhibitors based on 2-(benzylsulfinyl)benzoic acid scaffold

Rotondi, Giulia,Guglielmi, Paolo,Carradori, Simone,Secci, Daniela,De Monte, Celeste,De Filippis, Barbara,Maccallini, Cristina,Amoroso, Rosa,Cirilli, Roberto,Akdemir, Atilla,Angeli, Andrea,Supuran, Claudiu T.

, p. 1400 - 1413 (2019/08/26)

A large library of derivatives based on the scaffold of 2-(benzylsulfinyl)benzoic acid were synthesised and tested as atypical inhibitors against four different isoforms of human carbonic anhydrase (hCA I, II, IX and XII, EC 4.2.1.1). The exploration of the chemical space around the main functional groups led to the discovery of selective hCA IX inhibitors in the micromolar/nanomolar range, thus establishing robust structure-activity relationships within this versatile scaffold. HPLC separation of some selected chiral compounds and biological evaluation of the corresponding enantiomers was performed along with molecular modelling studies on the most active derivatives.

Synthesis of Spirofurooxindoles via Phenyliodine(III) Bis(trifluoroacetate) (PIFA)-Mediated Cascade Oxidative C?O and C?C Bond Formation

Sun, Desong,Zhao, Xiaoyuan,Zhang, Bobo,Cong, Ying,Wan, Xintong,Bao, Mingmai,Zhao, Xue,Li, Bing,Zhang-Negrerie, Daisy,Du, Yunfei

supporting information, p. 1634 - 1638 (2018/03/21)

Upon treatment with solely a hypervalent iodine reagent of phenyliodine(III) bis(trifluoroacetate) (PIFA), 3-(2-hydroxyphenyl)-3-oxo-N-phenyl propanamides and a series of its derivatives were conveniently converted to a class of undocumented spirofurooxindoles under mild conditions. Control experiments provided evidence that this spirocyclization process encompassed a cascade oxidative reactions involving the formation of a C?O bond prior to that of C?C bond. (Figure presented.).

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