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35031-72-2

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35031-72-2 Usage

General Description

4-Ethoxypropiophenone is a chemical compound with the formula C11H14O2. It is an organic compound that is used as a reagent in the synthesis of pharmaceuticals and other organic compounds. It is a clear, colorless liquid with a slight aromatic odor, and it is soluble in most organic solvents. 4-Ethoxypropiophenone is commonly used as an intermediate in the production of various chemicals and has applications in the pharmaceutical and food industries. It is important to handle 4-ethoxypropiophenone with caution, as it can be irritating to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 35031-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,3 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35031-72:
(7*3)+(6*5)+(5*0)+(4*3)+(3*1)+(2*7)+(1*2)=82
82 % 10 = 2
So 35031-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O2/c1-3-11(12)9-5-7-10(8-6-9)13-4-2/h5-8H,3-4H2,1-2H3

35031-72-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-ethoxyphenyl)propan-1-one

1.2 Other means of identification

Product number -
Other names 1-(4-Aethoxy-phenyl)-propan-1-on

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:35031-72-2 SDS

35031-72-2Relevant articles and documents

BR?NSTED-ACIDIC FLUOROALKYL PHOSPHONATES

-

Paragraph 0288-0290, (2018/10/04)

The invention relates to Br?nsted-acidic fluoroalkyl phosphonates as bifunctional catalysts and to processes for the preparation thereof.

Catalytic Friedel-Crafts acylation of alkoxybenzenes mediated by aluminum hydrogensulfate in solution and solvent-free conditions

Salehi, Peyman,Khodaei, Mohammad Mehdi,Zolfigol, Mohammad Ali,Sirouszadeh, Sara

, p. 1863 - 1864 (2007/10/03)

Friedel-Crafts acylation of alkoxybenzenes was achieved efficiently by a reaction with aliphatic acid anhydrides in the presence of catalytic amounts of aluminum hydrogensulfate, Al(HSO4)3, in nitromethane and under solvent-free conditions. Alkylbenzenes and aryl halides, as well as aromatic anhydrides, remained intact under these conditions.

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