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(S)-BoroLeu-(-)-Pinanediol-CF3COOH is a complex chemical compound that integrates three distinct components: BoroLeu, a boron-containing derivative of leucine; (-)-Pinanediol, a chiral auxiliary pivotal for stereocontrol in organic synthesis; and CF3COOH, a strong trifluoroacetic acid used extensively in organic chemistry. This unique amalgamation is likely to function as a reagent or chiral catalyst, facilitating the controlled and selective synthesis of chiral compounds. Its potential applications extend to the development of innovative pharmaceuticals and the creation of other chiral materials, making it a valuable asset in the field of organic chemistry and drug discovery.

477254-69-6

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477254-69-6 Usage

Uses

Used in Pharmaceutical Development:
(S)-BoroLeu-(-)-Pinanediol-CF3COOH is used as a chiral catalyst for the asymmetric synthesis of pharmaceutical compounds, leveraging its stereocontrol properties to produce enantiomerically pure products. This is crucial for the development of new drugs, as the biological activity of chiral molecules can vary significantly between enantiomers.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-BoroLeu-(-)-Pinanediol-CF3COOH serves as a reagent that aids in the selective formation of chiral centers in target molecules. Its role is vital for reactions where the stereochemistry of the product is essential for biological activity or to meet specific chemical requirements.
Used in Chiral Auxiliary Development:
(S)-BoroLeu-(-)-Pinanediol-CF3COOH is utilized as a chiral auxiliary in the synthesis of complex organic molecules, providing a stereochemical handle that can be introduced and later removed during the synthesis process. This application is particularly useful in total synthesis and the preparation of natural products with multiple stereocenters.
Used in Analytical Chemistry:
(S)-BoroLeu-(-)-Pinanediol-CF3COOH can be employed as a chiral derivatizing agent in analytical chemistry, helping to resolve enantiomeric mixtures and determine the enantiomeric purity of chiral compounds through techniques such as chromatography and mass spectrometry.
Used in Materials Science:
In materials science, (S)-BoroLeu-(-)-Pinanediol-CF3COOH may be used as a building block for the synthesis of chiral materials with specific properties, such as optical activity or the ability to interact differently with other chiral molecules. This can lead to advances in areas like sensors, catalysts, and materials with tailored interactions at the molecular level.

Check Digit Verification of cas no

The CAS Registry Mumber 477254-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,7,2,5 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 477254-69:
(8*4)+(7*7)+(6*7)+(5*2)+(4*5)+(3*4)+(2*6)+(1*9)=186
186 % 10 = 6
So 477254-69-6 is a valid CAS Registry Number.

477254-69-6SDS

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 (1S)-(S)-pinanediol 1-ammonium trifluoroacetate-3-methylbutane-1-boronate

1.2 Other means of identification

Product number -
Other names (1S)-(1S,2S,3R,5S)-pinanediol-1-ammoniumtrifluoroacetate-3-methylbutane-1-boronate

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:477254-69-6 SDS

477254-69-6Relevant academic research and scientific papers

SYNTHESIS OF BORONIC ESTER AND ACID COMPOUNDS

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Page/Page column 40-41, (2010/02/14)

The invention relates to the synthesis of boronic ester and acid compounds. More particularly, the invention provides improved synthetic processes for the large-scale production of boronic ester and acid compounds, including the peptide boronic acid proteasome inhibitor bortezomib.

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