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112753-55-6

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112753-55-6 Usage

Structure

A ketone with a furan ring and a phenyl group attached to the central carbon atom.

Type of compound

Organic compound

Usage

Building block in organic synthesis, used in various chemical reactions and processes.

Applications

Potential applications in pharmaceuticals, agrochemicals, and materials science.

Importance

Unique structure and reactivity make it a valuable intermediate in the production of various chemicals and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 112753-55-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,5 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112753-55:
(8*1)+(7*1)+(6*2)+(5*7)+(4*5)+(3*3)+(2*5)+(1*5)=106
106 % 10 = 6
So 112753-55-6 is a valid CAS Registry Number.

112753-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(5-methylfuran-2-yl)-3-phenylpropan-1-one

1.2 Other means of identification

Product number -
Other names 1-Propanone,1-(5-methyl-2-furanyl)-3-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:112753-55-6 SDS

112753-55-6Relevant articles and documents

An efficient heterogenized palladium catalyst for N-alkylation of amines and α-alkylation of ketones using alcohols

Dang, Tuan Thanh,Shan, Siah Pei,Ramalingam, Balamurugan,Seayad, Abdul Majeed

, p. 42399 - 42406 (2015/05/20)

A silica supported palladium-NiXantphos complex is reported as an efficient and a high turnover heterogeneous catalyst for the N-alkylation of amines and the α-alkylation of ketones using readily available alcohols under neat conditions at 120-140 °C following hydrogen borrowing strategy. The catalyst is easily separable and offers negligible amount of palladium leaching (0.01 ppm). A high turnover number of about 46000 for the N-alkylation of amines and 4400 for the α-alkylation of ketones were achieved in the respective single batch reactions. The catalyst is recyclable up to four times without appreciable change in catalytic performance.

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