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1287759-43-6

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1287759-43-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1287759-43-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,7,7,5 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1287759-43:
(9*1)+(8*2)+(7*8)+(6*7)+(5*7)+(4*5)+(3*9)+(2*4)+(1*3)=216
216 % 10 = 6
So 1287759-43-6 is a valid CAS Registry Number.

1287759-43-6Downstream Products

1287759-43-6Relevant articles and documents

Tunable poly(hydroxyl urethane) from CO2-Based intermediates using thiol-ene chemistry

Tang, Chau N.,Nulwala, Hunaid B.,Damodaran, Krishnan,Kaur, Palwinder,Luebke, David R.

experimental part, p. 2024 - 2032 (2012/03/26)

CO2-based, crosslinked poly(hydroxyl urethane)s (PHUs) are accessed via a set of efficient reactions based on the addition chemistry of thiol-ene and amines-cyclic carbonates. This strategy to utilize 5-membered cyclic carbonates produced from CO2 is robust, facile, modular, and atomically efficient in nature. The thiol-ene reaction was utilized to access bis(cyclic carbonate), tris(cyclic carbonate), and tetrakis(cyclic carbonate) in quantitative yield from 4-vinyl-1,3-dioxolan-2-one and thiols. Multi-functional cyclic carbonates were simply mixed with diethylenetriamine and/or 1,6-diaminohexane to generate crosslinked PHUs from 25 to 80 °C. These materials are easy to scale-up and are potential candidates in many applications such as coatings, binders, and resins. The resulting polymers have glass transition temperatures between -1 and 16 °C and thermal decomposition temperatures from 190 to 230 °C. 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 CO2-based, crosslinked poly(hydroxyl urethane)s (PHUs) are accessed via a set of efficient reactions based on the addition chemistry of thiol-ene and amines-cyclic carbonates. The thiol-ene reaction was utilized to access multi-functional cyclic carbonates in quantitative yield from 4-vinyl-1,3-dioxolan-2-one and thiols. These precursors were simply mixed with diethylenetriamine and/or 1,6-diaminohexane to generate crosslinked PHUs. Copyright

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