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2-Oxazolidinone,3-[(5S)-5-(4-fluorophenyl)-5-hydroxy-1-oxopentyl]-4-(phenylmethyl)-,(4S)is a complex organic compound characterized by a 4-(phenylmethyl) oxazolidinone backbone. It features a 5-(4-fluorophenyl) substituent at the 5th position of the oxazolidinone ring and a 5-hydroxy-1-oxopentyl group. 2-Oxazolidinone,3-[(5S)-5-(4-fluorophenyl)-5-hydroxy-1-oxopentyl]-4-(phenylmethyl)-,(4S)is chiral, with the (5S) and (4S) stereoisomers present. Its chemical structure, which includes a phenylmethyl substituent and a 4-fluorophenyl group, suggests potential pharmaceutical activity, particularly in the realm of antimicrobial and antibacterial properties.

852148-49-3

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  • (4S)-4-benzyl-3-[(5S)-5-(4-fluorophenyl)-5-hydroxypentanoyl]-1,3-oxazolidin-2-one

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852148-49-3 Usage

Uses

Used in Pharmaceutical Industry:
2-Oxazolidinone,3-[(5S)-5-(4-fluorophenyl)-5-hydroxy-1-oxopentyl]-4-(phenylmethyl)-,(4S)is used as a potential antimicrobial and antibacterial agent due to its oxazolidinone backbone, which is known for these properties. The presence of the 4-fluorophenyl and phenylmethyl substituents may enhance its biological activity, making it a candidate for further research and development in the pharmaceutical field.
Used in Medicinal Chemistry Research:
2-Oxazolidinone,3-[(5S)-5-(4-fluorophenyl)-5-hydroxy-1-oxopentyl]-4-(phenylmethyl)-,(4S)is used as a subject of study in medicinal chemistry research to explore its potential applications and effects. The unique combination of functional groups and stereochemistry in 2-Oxazolidinone,3-[(5S)-5-(4-fluorophenyl)-5-hydroxy-1-oxopentyl]-4-(phenylmethyl)-,(4S)may offer insights into the design of new drugs with improved efficacy and selectivity.
Further research and testing are necessary to fully understand the potential uses and effects of this chemical, as its complex structure and chirality may influence its interactions with biological targets and its overall pharmacological profile.

Check Digit Verification of cas no

The CAS Registry Mumber 852148-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,1,4 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 852148-49:
(8*8)+(7*5)+(6*2)+(5*1)+(4*4)+(3*8)+(2*4)+(1*9)=173
173 % 10 = 3
So 852148-49-3 is a valid CAS Registry Number.

852148-49-3SDS

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 (4S)-4-benzyl-3-[(5S)-5-(4-fluorophenyl)-5-hydroxypentanoyl]-1,3-oxazolidin-2-one

1.2 Other means of identification

Product number -
Other names (4S)-3-[(5S)-5-(4-Fluorophenyl)-5-hydroxy-1-oxopentyl]-4-(phenylmethyl)-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:852148-49-3 SDS

852148-49-3Downstream Products

852148-49-3Relevant articles and documents

Process For Production Of 4-Biphenylyazetidin-2-Ones

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Page/Page column 20-21, (2008/12/09)

The present invention relates to processes for the production of 4-biphenylylazetidin-2-one derivatives of formula

4-BIARYLYL-1-PHENYLAZETIDIN-2-ONES

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, (2010/11/25)

4-Biarylyl-1-phenylazetidin-2-ones useful for the treatment of hypercholesterolemia are disclosed.

DIPHENYLHETEROCYCLE CHOLESTEROL ABSORPTION INHIBITORS

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, (2008/06/13)

Various azetidinone, pyrrolidine, imidazolidine, and oxazolidine derivatives are described, as are pharmaceutical compositions containing these compounds and methods of treatment of diseases using these compounds. Other embodiments are also described.

PROCESSES FOR PRODUCTION OF PHENOLIC 4-BIPHENYLYLAZETIDIN-2-ONES

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Page/Page column 34-35, (2010/11/24)

The present invention relates to processes for the production of phenolic 4-biphenylylazetidin-2-one derivatives Formula (1)

PHENYLAZETIDINONE DERIVATIVES

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Page/Page column 246; 288-289, (2008/06/13)

Various azetidinone derivatives are described, as are pharmaceutical compositions containing these compounds and methods of treatment of diseases using these compounds. Other embodiments are also described.

4-BIARYLYL-1-PHENYLAZETIDIN-2-ONES

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Page/Page column 68-69, (2010/02/11)

4-Biarylyl-1-phenylazetidin-2-ones useful for the treatment of hypercholesterolemia are disclosed. The compounds are of a general formula (I) in which formula (II) represents an aryl or heteroaryl residue, Ar represents an aryl residue; U is a two to six atom chain; and the R’s represent substituents.

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