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(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-diphenyl-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1297613-72-9

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1297613-72-9 Usage

Uses

Used in Pharmaceutical Industry:
(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-diphenyl-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-oxide is used as a potential pharmaceutical candidate for [specific application reason, if available] due to its unique structure and the presence of functional groups that may exhibit biological activity.
Used in Organic Synthesis:
In the field of organic synthesis, (11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-diphenyl-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-oxide is used as a key intermediate or building block for the synthesis of other complex organic molecules, taking advantage of its unique structure and reactivity.
Used in Material Science:
(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-diphenyl-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-oxide is utilized in material science for the development of new materials with specific properties, such as optoelectronic materials, sensors, or catalysts,得益于其独特的结构和性质。

Check Digit Verification of cas no

The CAS Registry Mumber 1297613-72-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,7,6,1 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1297613-72:
(9*1)+(8*2)+(7*9)+(6*7)+(5*6)+(4*1)+(3*3)+(2*7)+(1*2)=189
189 % 10 = 9
So 1297613-72-9 is a valid CAS Registry Number.

1297613-72-9Downstream Products

1297613-72-9Relevant academic research and scientific papers

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

, 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;

Optically active 1,1′-Spirobiindane-7,7′-diol (SPINOL)-based phosphoric acids as highly enantioselective catalysts for asymmetric organocatalysis

Xing, Chun-Hui,Liao, Yuan-Xi,Ng, Jaclynn,Hu, Qiao-Sheng

experimental part, p. 4125 - 4131 (2011/07/07)

The synthesis and application of a series of optically active 1,1′-spirobiindane-7,7′-diol (SPINOL)-based phosphoric acids are described. These SPINOL-based phosphoric acids were prepared from (R)-SPINOL in three steps and exhibited excellent enantioselec

SPINOL-derived phosphoric acids: Synthesis and application in enantioselective Friedel-Crafts reaction of indoles with imines

Xu, Fangxi,Huang, Dan,Han, Chao,Shen, Wei,Lin, Xufeng,Wang, Yanguang

, p. 8677 - 8680 (2011/02/26)

A new class of chiral phosphoric acids with spirobiindane as scaffold were conveniently synthesized from (S)-1,1′-spirobiindane-7,7′-diol ((S)-SPINOL) and employed to catalyze the asymmetric Friedel-Crafts reaction of indoles with imines to afford 3-indol

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