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4,4′-(propane-2,2-diyl)bis((prop-1-en-1-yloxy)benzene) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96361-37-4

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96361-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96361-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,3,6 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96361-37:
(7*9)+(6*6)+(5*3)+(4*6)+(3*1)+(2*3)+(1*7)=154
154 % 10 = 4
So 96361-37-4 is a valid CAS Registry Number.

96361-37-4Relevant academic research and scientific papers

COMPOUND, CURABLE COMPOSITION INCLUDING THE SAME AND CROSSLINKING AGENT FOR CURABLE COMPOSITION

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Paragraph 0051-0054, (2021/07/17)

PROBLEM TO BE SOLVED: To provide a curable composition that yields a cured object with low dielectric constant and low dielectric loss tangent characteristics and exhibits viscosity excellent in handling ability, and a crosslinking agent suitable for the curable composition. SOLUTION: A curable composition includes a compound expressed by a following formula (1) and a polymaleimide compound. A curing agent including the compound expressed by the following formula (1) as a crosslinking agent comprises both high toughness and dielectric characteristic. In the following formula (1), R1 is independently an allyl group or a 1-propenyl group, R2 is independently a monovalent organic group, X is an organic group having n valence or an atom, or a single bond, m is an integer of 0 to 4, and n is an integer of 2-4. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

Understanding the reactivity of enol ether radical cations: Investigation of anodic four-membered carbon ring formation

Yamaguchi, Yusuke,Okada, Yohei,Chiba, Kazuhiro

, p. 2626 - 2638 (2013/04/23)

The reactivity of enol ether radical cations was investigated in anodic four-membered carbon ring formations, advancing the mechanistic understanding of these reactions. The mono-ring-containing aromatic cations were reduced through inter- or intramolecular electron transfer to give mono- or bis-ring-containing compounds, respectively. Small structural changes in the hydrocarbon linkers tethering two aromatic rings exerted a powerful effect on the efficiency of such electron transfer events.

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