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9-phenylnonane-4,6-diynoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

902760-14-9

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902760-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 902760-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,2,7,6 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 902760-14:
(8*9)+(7*0)+(6*2)+(5*7)+(4*6)+(3*0)+(2*1)+(1*4)=149
149 % 10 = 9
So 902760-14-9 is a valid CAS Registry Number.

902760-14-9Relevant academic research and scientific papers

Synthesis and self-assembling properties of diacetylene-containing glycolipids

Nie, Xiaoping,Wang, Guijun

, p. 4734 - 4741 (2006)

Diacetylene-containing glycolipids are interesting molecules that have many potential applications. The polydiacetylenes formed by the cross-linking of the diacetylene lipids are new stimuli-responsive materials. In particular, diacetylene lipids that can form gels in aqueous solution are of great interest in designing functional biocompatible materials. We have synthesized a series of diacetylene-containing sugar lipids with different chain lengths, substituents, and positions of diyne and studied their self-assembling properties in several solvents including hexane, ethanol, and ethanol/water mixture. Among the 24 diacetylene-containing glycolipids synthesized, many of them exhibited excellent gelation properties in ethanol or ethanol/water mixture. Typically very long chain diacetylene lipids formed gels in ethanol and hexane. Shorter chain diacetylene lipids and compounds with one free hydroxyl group can form gels in aqueous solution. The position of the diyne and chain length affect the self-assembling properties significantly. The systematic study of the gelation properties for diacetylene lipids with different lipid chains can help us to understand the structure requirement for the desired physical properties. Optical microscopy studies showed that the molecules form interesting architectures such as tubules, rods, sheets, and belts. The resulting organogels can also be cross-linked and give different colored polymerized gels depending on their structures.

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