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2-Furanmethanol, tetrahydro-5-methyl-, acetate, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138901-55-0

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138901-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138901-55-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,0 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138901-55:
(8*1)+(7*3)+(6*8)+(5*9)+(4*0)+(3*1)+(2*5)+(1*5)=140
140 % 10 = 0
So 138901-55-0 is a valid CAS Registry Number.

138901-55-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-5-methyltetrahydrofurfuryl acetate

1.2 Other means of identification

Product number -
Other names Acetic acid (2S,5R)-5-methyl-tetrahydro-furan-2-ylmethyl ester

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:138901-55-0 SDS

138901-55-0Downstream Products

138901-55-0Relevant academic research and scientific papers

CATALYTIC SYNTHESIS OF REDUCED FURAN DERIVATIVES

-

Paragraph 0066, (2014/11/13)

The present invention relates to catalytic synthesis of furan derivatives from alkoxymethylfurfural ethers or acyloxymethylfurfural esters. More particularly, the invention pertains to furan derivatives obtained by use of a multifunctional catalyst system to carry out both hydrogenation of furan starting material and hydrolysis of the reduced furan derivative in a single reaction. The process allows recovering and recycling of alcohol or acid from the reaction product.

Stereocontrolled Synthesis of Tetrahydrofurans and Tetrahydropyrans Using Thallium(III)-Induced Cyclizations

Michael, Joseph P.,Ting, Pauline C.,Bartlett, Paul A.

, p. 2416 - 2423 (2007/10/02)

Various substituted 4-alkenols undergo electrophilic cyclization with thallium(III) salts in a regio- and stereoselective manner. The organothallium intermediate is not isolated but undergoes dethallation with concomitant 1,2-oxygen migration, leading to

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