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2050-04-6

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2050-04-6 Usage

General Description

(Pentyloxy)benzene, also known as anisole, is a chemical compound with the molecular formula C6H5OC5H11. It is a clear, colorless liquid with a pleasant, aromatic odor. Anisole is commonly used as a solvent in various industrial processes and as a flavoring agent in the food and beverage industry. It is also used in the production of perfumes and as an intermediate in the synthesis of other organic compounds. Anisole is flammable and should be handled with care, but it is generally considered to have low toxicity and is not known to cause harmful effects in humans when used as directed.

Check Digit Verification of cas no

The CAS Registry Mumber 2050-04-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2050-04:
(6*2)+(5*0)+(4*5)+(3*0)+(2*0)+(1*4)=36
36 % 10 = 6
So 2050-04-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O/c1-2-3-7-10-12-11-8-5-4-6-9-11/h4-6,8-9H,2-3,7,10H2,1H3

2050-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name pentoxybenzene

1.2 Other means of identification

Product number -
Other names 1-pentyl phenyl ether

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:2050-04-6 SDS

2050-04-6Relevant articles and documents

Selectivity engineering of phase transfer catalyzed alkylation of 2′-hydroxyacetophenone: Enhancement in rates and selectivity by creation of a third liquid phase

Yadav, Ganapati D.,Desai, Neesha M.

, p. 749 - 756 (2005)

Enhancements in rate of reaction and selectivity of the desired product in biphasic reactions are achieved by creating a third liquid phase, under appropriate conditions, where the third liquid phase is the locale of the main reaction, having a dramatic effect on product distribution in complex chemical reactions. Thus, in the case of phase transfer catalysis (PTC), conversion of liquid-liquid (L-L) PTC into liquid-liquid-liquid (L-L-L) PTC is of considerable techno-commercial interest resulting in waste minimization which is a major theme of green chemistry. Etherification of 2′-hydroxyacetophenone with 1-bromopentane, under traditional liquid-liquid phase transfer catalysis, results in loss of catalyst. However, the transformation of two liquid phases into three liquid phases (L-L-L) PTC leads enhancement in rates by orders of magnitude, with 100% conversion of the limiting reactant 1-bromopentane and 100% selectivity to 2′-pentyloxyacetophenone. This strategy eliminates separation problems and results in high reaction rates reducing the total reaction time. Moreover, the catalyst-rich third phase is recycled more than 7 times without loss in activity. The kinetics of the reaction are studied in great detail. There is a substantial reduction in activation energy under L-L-L PTC vis-a-vis L-L PTC, where the locale of the reaction is shifted from the organic phase to the third phase.

Cellulose oxidation and the use of carboxyl cellulose metal complexes in heterogeneous catalytic systems to promote suzuki-miyaura coupling and C?O bond formation reaction

Martins, Guilherme B. C.,Dos Santos, Marcelo R.,Rodrigues, Marcus V. R.,Sucupira, Renata R.,Meneghetti, Luisa,Monteiro, Adriano L.,Suarez, Paulo A. Z.

, p. 2064 - 2072 (2017/09/23)

This work shows the modification of microcrystalline cellulose by the selective oxidation of primary hydroxyl groups to carboxylate groups by a 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO)-mediated system and its application as a heterogeneous ligand by ionic exchange with catalytic metals ions such as palladium, nickel and copper. Afterwards is described the application of the synthesized material as catalyst in coupling reactions such as Suzuki-Miyaura coupling and C?O bond formation reaction in different conditions, which are of great importance for the synthesis of drugs, natural products and new materials such as dendrimers, liquid crystals and polymers with magnetic and optical properties. The carboxyl cellulose matrix shows to have superior catalytic results as a ligand for all coupling reactions. Can be also highlighted the affinity of the carboxyl cellulose ligand in polar solvents such as water and alcohols and its application in mild conditions.

Room temperature, metal-free arylation of aliphatic alcohols

Ghosh, Raju,Lindstedt, Erik,Jalalian, Nazli,Olofsson, Berit

, p. 54 - 57 (2014/05/06)

Diaryliodonium salts are demonstrated as efficient arylating agents of aliphatic alcohols under metal-free conditions. The reaction proceeds at room temperature within 90 min to give alkyl aryl ethers in good to excellent yields. Aryl groups with electron

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