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2-Butenoic acid, 4,4-diethoxy-, ethyl ester, (E)- is a chemical compound with the molecular formula C10H18O4. It is an ester derivative of 2-butenoic acid, featuring a double bond in the (E)-configuration, which means the substituents are on opposite sides of the double bond. The compound is characterized by the presence of two ethoxy groups attached to the 4-position of the butenoic acid backbone. This organic ester is known for its potential applications in the synthesis of various chemical products and as an intermediate in the production of pharmaceuticals and other specialty chemicals. Its structure and properties make it a versatile building block in organic chemistry, although specific uses and safety considerations should be consulted from detailed chemical databases and safety data sheets.

2960-65-8

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2960-65-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2960-65-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,6 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2960-65:
(6*2)+(5*9)+(4*6)+(3*0)+(2*6)+(1*5)=98
98 % 10 = 8
So 2960-65-8 is a valid CAS Registry Number.

2960-65-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4,4-diethoxybut-2-enoate

1.2 Other means of identification

Product number -
Other names Aethyl-4,4-diaethoxycrotonat

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:2960-65-8 SDS

2960-65-8Relevant academic research and scientific papers

SYNTHESE STEREOSELECTIVE DU DECADIENE-2(E), 4(Z)OATE D'ETHYLE. A PARTIR D'UN MONOACETAL DU GLYOXAL

Stambouli, A.,Amouroux, R.,Chastrette, M.

, p. 5301 - 5302 (1987)

The glyoxal monoacetal 2, now readily available in bulk quantity, is a very useful synthon for the dienes-1,3 synthesis, as illustrated in the stereoselective preparation of ethyl 2E,4Z-decadienoate using two Wittig-type olefination reactions.

DISSYMETRATION DE LA MOLECULE DU GLYOXAL 1-SYNTHESE ET REACTIVITE DE L'ACETOXY-1 TRIETHOXY-1,2,2 ETHANE

Stambouli, A.,Chastrette, F.,Amouroux, R.,Chastrette, M.,Mattioda, G.,Blanc, A.

, p. 4149 - 4152 (2007/10/02)

Acetoxy-1 triethoxy-1,2,2 ethane, a dissymetric derivative of glyoxal, is prepared and reacted with various bases and nucleophiles, as amines, cyanotrimethylsilane, organometallic and WITTIG reagents.Various acetals are obtained, leading to α-fonctionalized aldehydes.

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