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203000-59-3

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  • (S,S)-1,2-Bis[(tert-butyl)methylphosphino]ethane(norbornadiene)rhodium(I) tetrafluoroborate

    Cas No: 203000-59-3

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  • (S,S)-1,2-BIS[(TERT-BUTYL)METHYLPHOSPHINO]ETHANE[ETA-(2,5-NORBORNADIENE)]RHODIUM(I) TETRAFLUOROBORATE

    Cas No: 203000-59-3

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203000-59-3 Usage

Description

(S,S)-1,2-BIS[(TERT-BUTYL)METHYLPHOSPHINO]ETHANE[ETA-(2,5-NORBORNADIENE)]RHODIUM(I) TETRAFLUOROBORATE is a chemical compound that features a rhodium(I) center coordinated to a chelating ligand and a norbornadiene ligand. The chelating ligand, (S,S)-1,2-bis[(tert-butyl)methylphosphino]ethane, is known for its stabilizing properties in organometallic chemistry, while the norbornadiene ligand is a versatile diene capable of participating in cycloaddition reactions with unsaturated substrates. The tetrafluoroborate anion serves to balance the positive charge of the rhodium center, making this compound a potent catalyst in various organic reactions.

Uses

Used in Organic Synthesis:
(S,S)-1,2-BIS[(TERT-BUTYL)METHYLPHOSPHINO]ETHANE[ETA-(2,5-NORBORNADIENE)]RHODIUM(I) TETRAFLUOROBORATE is used as a catalyst for C-H activation, enabling the conversion of unactivated C-H bonds into more reactive C-X bonds (where X can be a variety of functional groups), which is crucial for the synthesis of complex organic molecules.
Used in Hydrogenation Reactions:
In the field of hydrogenation, this compound serves as a catalyst to facilitate the reduction of unsaturated organic compounds (such as alkenes and alkynes) to their corresponding saturated hydrocarbons, which is essential for the production of various chemicals and pharmaceuticals.
Used in Cycloaddition Reactions:
(S,S)-1,2-BIS[(TERT-BUTYL)METHYLPHOSPHINO]ETHANE[ETA-(2,5-NORBORNADIENE)]RHODIUM(I) TETRAFLUOROBORATE is used as a catalyst in cycloaddition reactions, which are fundamental processes in organic chemistry for creating cyclic compounds from unsaturated molecules. This is particularly important in the synthesis of complex organic structures and natural products.
Used in the Pharmaceutical Industry:
In the pharmaceutical sector, this compound is utilized as a catalyst for various organic transformations that are critical in the synthesis of active pharmaceutical ingredients, enhancing the efficiency and selectivity of these processes.
Used in the Chemical Industry:
The chemical industry employs (S,S)-1,2-BIS[(TERT-BUTYL)METHYLPHOSPHINO]ETHANE[ETA-(2,5-NORBORNADIENE)]RHODIUM(I) TETRAFLUOROBORATE as a catalyst in the production of various chemical intermediates and final products, contributing to the advancement of material science and the development of new compounds with specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 203000-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,0,0 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 203000-59:
(8*2)+(7*0)+(6*3)+(5*0)+(4*0)+(3*0)+(2*5)+(1*9)=53
53 % 10 = 3
So 203000-59-3 is a valid CAS Registry Number.

203000-59-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo[2.2.1]hepta-2,5-diene,tert-butyl-[2-[tert-butyl(methyl)phosphanyl]ethyl]-methylphosphane,rhodium,tetrafluoroborate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:203000-59-3 SDS

203000-59-3Upstream product

203000-59-3Downstream Products

203000-59-3Relevant articles and documents

P-chiral bis(trialkylphosphine) ligands and their use in highly enantioselective hydrogenation reactions [9]

Imamoto,Watanabe,Wada,Masuda,Yamada,Tsuruta,Matsukawa,Yamaguchi

, p. 1635 - 1636 (2007/10/03)

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