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1412439-82-7

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  • (11aS)-3,7-Bis(3,5-dimethylphenyl)-10,11,12,13-tetrahydro-5-hydroxy-5-oxide-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin, min. 98%

    Cas No: 1412439-82-7

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  • (11aS)-3,7-Bis(3,5-dimethylphenyl)-10,11,12,13-tetrahydro-5-hydroxy-5-oxide-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin

    Cas No: 1412439-82-7

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1412439-82-7 Usage

General Description

(11aS)-5-oxide-3,7-bis(3,5-diMethylphenyl)-10,11,12,13-tetrahydro-5-hydroxy-Diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin is a complex chemical compound with a long and detailed name. It is a phosphorous-containing organic compound with a unique structure, including a tetrahydro and diindeno ring system. (11aS)-5-oxide-3,7-bis(3,5-diMethylphenyl)-10,11,12,13-tetrahydro-5-hydroxy-Diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin is also a derivative of dioxaphosphocin, containing multiple methyl and hydroxyl groups. Its structure and functional groups make it a potentially versatile chemical for specific applications, but further analysis and study would be necessary to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 1412439-82-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,2,4,3 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1412439-82:
(9*1)+(8*4)+(7*1)+(6*2)+(5*4)+(4*3)+(3*9)+(2*8)+(1*2)=137
137 % 10 = 7
So 1412439-82-7 is a valid CAS Registry Number.

1412439-82-7Downstream Products

1412439-82-7Relevant articles and documents

Asymmetric Ni-H insertion reaction cooperatively catalyzed by rhodium and chiral spiro phosphoric acids

Xu, Bin,Zhu, Shou-Fei,Xie, Xiu-Lan,Shen, Jun-Jie,Zhou, Qi-Lin

supporting information; experimental part, p. 11483 - 11486 (2012/01/11)

So near so SPA: Achiral dirhodium(II) carboxylates and chiral spiro phosphoric acids (SPA) cooperatively catalyzed asymmetric Ni-H insertion reactions with high enantioselectivity, high yields, and fast reaction rates at low catalyst loading (see scheme;

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