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2(3H)-Furanone, dihydro-3-(3-methylphenoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31145-62-7

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31145-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31145-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,4 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 31145-62:
(7*3)+(6*1)+(5*1)+(4*4)+(3*5)+(2*6)+(1*2)=77
77 % 10 = 7
So 31145-62-7 is a valid CAS Registry Number.

31145-62-7SDS

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 3-(3-methylphenoxy)oxolan-2-one

1.2 Other means of identification

Product number -
Other names 3-m-tolyloxy-dihydro-furan-2-one

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:31145-62-7 SDS

31145-62-7Downstream Products

31145-62-7Relevant academic research and scientific papers

Preparation method of 3,4-dihydro-2H-1-benzopyran-2-carboxylic acid compound and application thereof

-

Paragraph 0045; 0048; 0049, (2018/07/15)

Disclosed are a preparation method of a 3,4-dihydro-2H-1-benzopyran-2-carboxylic acid compound and application thereof. The invention relates to the field of organic synthesis. According to the method, a phenolic compound is reacted with a gamma-butyrrolactone compound under the action of alkalis to obtain an intermediate; ring-closing reaction is conducted on the intermediate under the action ofacid catalysts, and the 3,4-dihydro-2H-1-benzopyran-2-carboxylic acid compound is obtained with high efficiency and high yield only by two simple steps of reaction; the preparation method has the advantages of being simple in routine design and procedures, convenient to operate and low in cost, and the method is very suitable for industrialized large-scale production; by applying the preparation method of the 3,4-dihydro-2H-1-benzopyran-2-carboxylic acid compound to the application for preparing medicines with the structure of 3,4-dihydro-2H-1-benzopyran-2-carboxylic acid, the yield of the medicines can be improved and the production cost can be reduced.

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