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5460-45-7

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5460-45-7 Usage

Description

2-Ethylhexyl formate is a colorless liquid chemical compound with the formula C10H20O2. It is an ester formed by the condensation of 2-ethylhexanol and formic acid, characterized by its fruity odor.

Uses

Used in Flavoring Industry:
2-Ethylhexyl formate is used as a flavoring agent for its distinctive fruity scent, enhancing the taste and aroma of various food products.
Used in Chemical Production:
2-Ethylhexyl formate serves as a solvent and intermediate in the production of different chemicals, contributing to the synthesis of a wide range of compounds.
Used in Solvent Applications:
As a solvent, 2-Ethylhexyl formate is utilized in various industrial processes, aiding in the dissolution and handling of other substances for manufacturing purposes.
Safety Note:
Due to its flammable nature, 2-Ethylhexyl formate should be handled with care and proper safety measures should be followed to minimize the risk of exposure and adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 5460-45-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5460-45:
(6*5)+(5*4)+(4*6)+(3*0)+(2*4)+(1*5)=87
87 % 10 = 7
So 5460-45-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O2/c1-3-5-6-9(4-2)7-11-8-10/h8-9H,3-7H2,1-2H3

5460-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylhexyl formate

1.2 Other means of identification

Product number -
Other names Formiat des 2-Ethylhexanols

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:5460-45-7 SDS

5460-45-7Downstream Products

5460-45-7Relevant articles and documents

ETHERIFICATION PROCESS

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Page/Page column 25, (2019/05/10)

The present invention relates to a process for preparing ethers, particularly unsymmetrical ethers, and preferably ethers suitable for use as base stocks for lubricant compositions. In particular, the process involves the reaction of an α,β-unsaturated aldehyde with a trihydrocarbyl orthoester to form an α,β-unsaturated acetal and conversion of the α,β- unsaturated acetal to an ether through hydrogenation and hydrogenolysis.

Formamides as Lewis Base Catalysts in SNReactions—Efficient Transformation of Alcohols into Chlorides, Amines, and Ethers

Huy, Peter H.,Motsch, Sebastian,Kappler, Sarah M.

supporting information, p. 10145 - 10149 (2016/08/16)

A simple formamide catalyst facilitates the efficient transformation of alcohols into alkyl chlorides with benzoyl chloride as the sole reagent. These nucleophilic substitutions proceed through iminium-activated alcohols as intermediates. The novel method, which can be even performed under solvent-free conditions, is distinguished by an excellent functional group tolerance, scalability (>100 g) and waste-balance (E-factor down to 2). Chiral substrates are converted with excellent levels of stereochemical inversion (99 %→≥95 % ee). In a practical one-pot procedure, the primary formed chlorides can be further transformed into amines, azides, ethers, sulfides, and nitriles. The value of the method was demonstrated in straightforward syntheses of the drugs rac-Clopidogrel and S-Fendiline.

Efficient one-step conversion of tetrahydropyranyl ethers into acetates and formates in the presence of potassium dodecatungstocobaltate K 5CoW12O40·3H2O

Rafiee,Tangestaninejad,Habibi,Mohammadpoor-Baltork,Mirkhani

, p. 393 - 395 (2007/10/03)

Tetrahydropyranyl ethers derived from primary alcohols were directly and efficiently converted into the corresponding acetates and formates by the action of ethyl acetate, acetic acid, acetic anhydride, and ethyl formate in the presence of a catalytic amount of potassium dodecatungstocobaltate K 5CoW12O40 ? 3H2O. Tetrahydropyranyl ethers derived from secondary alcohols and phenols can also be transformed into the corresponding acetates with the use of acetic anhydride, but K5CoW12O40 ? 3H2O was ineffective for esterification with ethyl acetate, acetic acid, and ethyl formate.

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