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Endo-Δ1,3-Cyclohexadien-Maleinsaeure-anhydrid-Addukt, also known as Endo-Δ1,3-cyclohexadiene-maleic anhydride adduct, is a chemical compound derived from the reaction between maleic anhydride and cyclohexadiene. This adduct is characterized by its unique endo-Δ1,3-cyclohexadiene structure, which is formed by the addition of maleic anhydride to the double bonds of cyclohexadiene. The compound exhibits interesting properties and potential applications in various fields, such as polymer chemistry and material science, due to its ability to form stable complexes and its reactivity with other molecules. The specific structure and properties of this adduct make it a subject of interest for researchers studying the behavior of organic compounds and their potential uses in industrial applications.

3769-13-9

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3769-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3769-13-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,6 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3769-13:
(6*3)+(5*7)+(4*6)+(3*9)+(2*1)+(1*3)=109
109 % 10 = 9
So 3769-13-9 is a valid CAS Registry Number.

3769-13-9Relevant academic research and scientific papers

Catalyst economy. Part 2: Sequential metathesis - Kharasch sequences using the Grubbs metathesis catalysts

Edlin, Chris D.,Faulkner, James,Quayle, Peter

, p. 1145 - 1151 (2006)

Sequential ring-closing metathesis (RCM)-Kharasch cyclizations are promoted by the Grubbs metathesis catalysts and provide rapid access to bicyclic lactones and lactams.

PHARMACEUTICAL COMPOSITION FOR USE IN THE TREATMENT AND PREVENTION OF ORTHOPOXVIRUS INFECTIONS AND ASSOCIATED DISEASES

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Paragraph 0095; 0096, (2016/08/03)

Pharmaceutical compositions containing di, tri, and tetracyclic acylhydrazide derivatives of the formula below, for use in the treatment or prophylaxis of viral infections and diseases associated therewith, particularly those viral infections and associated diseases caused by the orthopoxvirus.

A Remarkably Efficient Photochemical Methodology for Endo to Exo Isomerization of Diels-Alder Cycloadducts

Pandey, Bipin,Athawale, Asawari A.,Reddy, Ravinder S.,Dalvi, Pramod V.,Kumar, Pradeep

, p. 1173 - 1176 (2007/10/02)

Irradiation of a solution of ethanol containing Diels-Alder cycloadducts and 10-20 percent (by volume) triethylamine at 300 nm furnishes quantitative yield (>90percent) of corresponding exo isomers.A probable mechanism based on photo-induced electron transfer (PET) has been described.

Synthesis of exo-Bicyclooct-5-ene-dicarboxylic Anhydrides by Thermal Isomerization of trans-Diacids

Weisz, Adrian,Mandelbaum, Asher

, p. 5812 - 5815 (2007/10/02)

Bicyclooct-5-ene-trans-1,2-dicarboxylic acid and substituted analogues afford mixtures of the corresponding exo- and endo-anhydrides upon heating at 250-300 deg C.This isomerization provides a practical pathway to substituted and deuterium-labeled exo-anhydrides which are otherwise difficult to obtain.A mechanistic study shows that retro-diene fragmentation is not involved in the isomerization.

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