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2,6-bis(4,4-dimethyl-4,5-dihydro-1,3-oxazol-2-yl)pyridine, commonly referred to as BOP, is a prominent chemical compound extensively utilized in the realm of organic synthesis. As a bidentate ligand, BOP is frequently employed in coordination chemistry and serves as a chiral auxiliary in asymmetric synthesis. Its capacity to form stable and highly selective complexes with transition metals renders it an indispensable tool in catalytic reactions. The distinctive structural attributes of BOP, which include two oxazoline rings and a pyridine core, endow it with a diverse reactivity profile and the capability to mediate a broad spectrum of synthetic transformations. In essence, BOP stands as a significant and adaptable chemical reagent, pivotal in the advancement of innovative and efficient synthetic strategies.

131864-69-2

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131864-69-2 Usage

Uses

Used in Coordination Chemistry:
2,6-bis(4,4-dimethyl-4,5-dihydro-1,3-oxazol-2-yl)pyridine is used as a bidentate ligand for the formation of stable and highly selective complexes with transition metals. This application is crucial in coordination chemistry due to BOP's ability to enhance the stability and selectivity of metal complexes, thereby facilitating a range of catalytic and stoichiometric reactions.
Used in Asymmetric Synthesis:
In the field of asymmetric synthesis, 2,6-bis(4,4-dimethyl-4,5-dihydro-1,3-oxazol-2-yl)pyridine is utilized as a chiral auxiliary. Its role is to induce chirality in the products of chemical reactions, which is vital for the synthesis of enantiomerically pure compounds, a key requirement in the production of pharmaceuticals and agrochemicals where stereochemistry plays a critical role in biological activity.
Used in Catalytic Reactions:
2,6-bis(4,4-dimethyl-4,5-dihydro-1,3-oxazol-2-yl)pyridine is employed as a ligand in catalytic reactions to improve the efficiency and selectivity of the processes. Its unique structure allows for the fine-tuning of catalytic systems, leading to enhanced reaction rates and yields, as well as greater control over product stereochemistry.
Used in the Development of Synthetic Methodologies:
In the broader scope of synthetic chemistry, 2,6-bis(4,4-dimethyl-4,5-dihydro-1,3-oxazol-2-yl)pyridine is used as a versatile reagent to develop new synthetic methodologies. Its diverse reactivity and capacity to participate in a wide array of synthetic transformations make it a valuable component in the creation of novel and efficient synthetic routes to complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 131864-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,8,6 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 131864-69:
(8*1)+(7*3)+(6*1)+(5*8)+(4*6)+(3*4)+(2*6)+(1*9)=132
132 % 10 = 2
So 131864-69-2 is a valid CAS Registry Number.

131864-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-bis[4’,4’-dimethyloxazolin-2’-yl]pyridine

1.2 Other means of identification

Product number -
Other names .2,6-bis[4',4'-dimethyloxazolin-2'-yl]pyridine

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 -
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More Details:131864-69-2 SDS

131864-69-2Relevant academic research and scientific papers

Oxidative-addition reactions of alkyl chlorides with chlorobis(cyclooctene)rhodium(I) and the bis(oxazolinyl)pyridine ligand: Formation of stable (chloromethyl)rhodium(III) complexes and their reactions

Nishiyama, Hisao,Horihata, Mihoko,Hirai, Tsuyoshi,Wakamatsu, Shigeru,Itoh, Kenji

, p. 2706 - 2708 (2008/10/08)

Dichloromethane and chloroform readily react with chlorobis(cyclooctene)rhodium(I) (1) and 2,6-bis-(4,4-dimethyloxazolin-2-yl)pyridine, dm-pybox, at room temperature to give the stable (chloromethyl)rhodium(III) complex 2 and (dichloromethyl)rhodium(III)

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