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(4S,5R)-(-)-4-i-propyl-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)-2-oxazolidinone, 99% is a chiral fluorous support used in organic synthesis. It is known for inducing high stereoselectivity in various reactions, including aldol reactions, cycloadditions, and conjugate additions involving N-acyl derivatives. The presence of a fluorous chain allows for rapid and efficient product isolation through solid phase extraction, using minimal amounts of common solvents. Additionally, it belongs to a class of catalytic ligands that exhibit enantioselectivity in the reduction of a wide range of substrates when used with a reducing agent.

871210-22-9

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871210-22-9 Usage

Uses

Used in Pharmaceutical Industry:
(4S,5R)-(-)-4-i-propyl-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)-2-oxazolidinone, 99% is used as a chiral fluorous support for enhancing stereoselectivity in the synthesis of pharmaceutical compounds. Its ability to induce high stereoselectivity in various reactions helps in the production of enantiomerically pure drugs, which is crucial for ensuring the desired therapeutic effects and minimizing potential side effects.
Used in Chemical Research:
In the field of chemical research, (4S,5R)-(-)-4-i-propyl-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)-2-oxazolidinone, 99% serves as a valuable tool for studying reaction mechanisms and developing new synthetic methodologies. Its enantioselective properties make it an attractive candidate for exploring asymmetric catalysis and the development of novel chiral catalysts.
Used in Environmentally Friendly Synthesis:
(4S,5R)-(-)-4-i-propyl-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)-2-oxazolidinone, 99% is used as a green chemistry reagent for reducing the environmental impact of chemical synthesis. The fluorous chain allows for efficient product isolation using minimal amounts of common solvents, thereby reducing waste and the need for hazardous solvents.
Used in High-Throughput Screening:
In the context of high-throughput screening, (4S,5R)-(-)-4-i-propyl-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)-2-oxazolidinone, 99% is employed as a chiral fluorous support for rapidly evaluating the stereoselectivity of various reactions. This enables chemists to identify the most promising synthetic routes and optimize reaction conditions more efficiently.

Check Digit Verification of cas no

The CAS Registry Mumber 871210-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,2,1 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 871210-22:
(8*8)+(7*7)+(6*1)+(5*2)+(4*1)+(3*0)+(2*2)+(1*2)=139
139 % 10 = 9
So 871210-22-9 is a valid CAS Registry Number.

871210-22-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Oxazolidinone, 4-(1-methylethyl)-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)-, (4S,5R)-

1.2 Other means of identification

Product number -
Other names (4S,5R)-(-)-4-I-PROPYL-5-(3,3,4,4,5,5,6,6,7,7,8,8,8-TRIDECAFLUOROOCTYL)-2-OXAZOLIDINONE

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:871210-22-9 SDS

871210-22-9Downstream Products

871210-22-9Relevant academic research and scientific papers

Practical synthesis of fluorous oxazolidinone chiral auxiliaries from α-amino acids

Hein, Jason E.,Geary, Laina M.,Jaworski, Ashley A.,Hultin, Philip G.

, p. 9940 - 9946 (2007/10/03)

A series of new fluorous-supported oxazolidinone chiral auxiliaries has been prepared using a versatile and general five-step pathway, starting from readily available chiral α-amino acids. The key feature of this synthesis is the efficient generation of a suitably active perfluoroalkyllithium species. By use of this protocol, the auxiliaries can be obtained in high enantiomeric purity and on multigram scales from L-phenylalanine and L-valine with overall yields as high as 55%. The new methodology also incorporates fluorous solid-phase extraction on the large scale, allowing bulk quantities (up to 25 g) of fluorous compounds to be purified from the crude reaction mixture.

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