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1309607-02-0

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1309607-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1309607-02-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,6,0 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1309607-02:
(9*1)+(8*3)+(7*0)+(6*9)+(5*6)+(4*0)+(3*7)+(2*0)+(1*2)=140
140 % 10 = 0
So 1309607-02-0 is a valid CAS Registry Number.

1309607-02-0Downstream Products

1309607-02-0Relevant articles and documents

Anhydrous TEMPO-H: Reactions of a good hydrogen atom donor with low-valent carbon centres

Giffin, Nick A.,Makramalla, Miller,Hendsbee, Arthur D.,Robertson, Katherine N.,Sherren, Cody,Pye, Cory C.,Masuda, Jason D.,Clyburne, Jason A. C.

, p. 3672 - 3680 (2011)

In this paper, we report a novel synthesis of anhydrous 1-hydroxy-2,2,6,6-tetramethyl-piperidine (TEMPO-H). An X-ray crystal structure and full characterization of the compound are included. Compared to hydrated TEMPO-H, its anhydrous form exhibits improved stability and a differing chemical reactivity. The reactions of anhydrous TEMPO-H with a variety of low-valent carbon centres are described. For example, anhydrous TEMPO-H was reacted with 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene (IMes), an unsaturated NHC. Crystals of [CHNC6H2(CH3)3] 2C...HO(NC5H6(CH3) 4), IMes...TEMPO-H, were isolated and a crystal structure determined. The experimental structure is compared to the results of theoretical calculations on the hydrogen-bonded dimer. Anhydrous TEMPO-H was also reacted with the saturated NHC, 1,3-bis(2,6-diisopropylphenyl)imidazolidin-2-ylidene (SIPr), giving the product [CH2Ni-Pr2C6H 3]2CH...O(NC5H6(CH 3)4). In contrast, the reaction of hydrated TEMPO-H with 1,3-bis(2,6-diisopropylphenyl)imidazolidin-2-ylidene gave small amounts of the hydrolysis product, N-(2,6-diisopropylphenyl)-N-[2-(2,6-diisopropylphenylamino) ethyl]formamide. Finally, anhydrous TEMPO-H was reacted with (triphenylphosphoranylidene)ketene to generate Ph3PC(H)C(O)O(NC 5H6(CH3)4). A full characterization of the product, including an X-ray crystal structure, is described.

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