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957782-11-5

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  • (R)-(-)-4,12-BIS(DI(3,5-XYLYL)PHOSPHINO)-[2.2]-PARACYCLOPHANE

    Cas No: 957782-11-5

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957782-11-5 Usage

Description

(R)-(-)-4,12-BIS(DI(3,5-XYLYL)PHOSPHINO)-[2.2]-PARACYCLOPHANE is a chiral phosphine ligand with a unique molecular structure, featuring a paracyclophane backbone and two phosphine groups attached to the para-positions of the xylyl groups. (R)-(-)-4,12-BIS(DI(3,5-XYLYL)PHOSPHINO)-[2.2]-PARACYCLOPHANE is known for its ability to efficiently bind to transition metal ions and induce stereoselectivity in chemical reactions, making it a valuable tool in the synthesis of complex organic molecules.

Uses

Used in Organometallic Chemistry:
(R)-(-)-4,12-BIS(DI(3,5-XYLYL)PHOSPHINO)-[2.2]-PARACYCLOPHANE is used as a catalyst in organometallic chemistry for various asymmetric reactions. Its chiral nature and efficient binding to transition metal ions enable the synthesis of complex organic molecules with high stereoselectivity.
Used in Pharmaceutical Industry:
(R)-(-)-4,12-BIS(DI(3,5-XYLYL)PHOSPHINO)-[2.2]-PARACYCLOPHANE is used as a catalyst for the synthesis of chiral pharmaceutical compounds. (R)-(-)-4,12-BIS(DI(3,5-XYLYL)PHOSPHINO)-[2.2]-PARACYCLOPHANE's ability to induce stereoselectivity in chemical reactions is crucial for the production of enantiomerically pure drugs, which can have different biological activities and reduce the risk of side effects.
Used in Chemical Research and Development:
(R)-(-)-4,12-BIS(DI(3,5-XYLYL)PHOSPHINO)-[2.2]-PARACYCLOPHANE is used as a research tool in the development of new synthetic methods and processes. Its unique molecular structure and catalytic properties make it an essential component in the design and optimization of novel chemical reactions and the synthesis of complex organic molecules.
Used in Material Science:
(R)-(-)-4,12-BIS(DI(3,5-XYLYL)PHOSPHINO)-[2.2]-PARACYCLOPHANE is used as a catalyst in the development of new materials with specific properties, such as chiral polymers and other advanced materials. (R)-(-)-4,12-BIS(DI(3,5-XYLYL)PHOSPHINO)-[2.2]-PARACYCLOPHANE's ability to induce stereoselectivity in chemical reactions can lead to the creation of materials with unique properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 957782-11-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,7,8 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 957782-11:
(8*9)+(7*5)+(6*7)+(5*7)+(4*8)+(3*2)+(2*1)+(1*1)=225
225 % 10 = 5
So 957782-11-5 is a valid CAS Registry Number.

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