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Diethyl 2,3-diethoxybutanedioate is a chemical compound with the molecular formula C10H18O6. It is an organic ester derived from butanedioic acid (succinic acid) and diethyl ether. diethyl 2,3-diethoxybutanedioate is characterized by its symmetrical structure, featuring two ethoxy groups attached to the central butanedioate core. It is a colorless liquid with a low melting point and is soluble in most organic solvents. Diethyl 2,3-diethoxybutanedioate is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its properties, such as its reactivity and solubility, make it a valuable building block in organic chemistry, particularly in the formation of complex molecules through esterification and condensation reactions.

7153-16-4

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7153-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7153-16-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7153-16:
(6*7)+(5*1)+(4*5)+(3*3)+(2*1)+(1*6)=84
84 % 10 = 4
So 7153-16-4 is a valid CAS Registry Number.

7153-16-4SDS

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 diethyl 2,3-diethoxybutanedioate

1.2 Other means of identification

Product number -
Other names di-O-ethyl-DL-tartaric acid diethyl 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:7153-16-4 SDS

7153-16-4Downstream Products

7153-16-4Relevant academic research and scientific papers

Veretherungen von Diolen, Triolen und Hydroxycarbonsaeurederivaten ueber Thallium(I)-alkoholate. Eine neue Variante der Williamson-Reaktion

Kalinowski, Hans-Otto,Crass, Gerhard,Seebach, Dieter

, p. 477 - 487 (2007/10/02)

The etherifications listed in tables 1 and 2 are achieved by converting hydroxy-derivatives, which contain additional oxygen functions, into thallium(I) alkoxides with thallium ethoxide, and treatment with haloalkanes.The scope and limitations of the method are discussed.

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