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(4S)-3-[(2S,4S)-4-Azido-2-(1-Methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-2-Oxazolidinone is a complex chemical compound with a unique molecular structure. It is characterized by the presence of a 4-azido group, oxazolidinone, furanyl moieties, and a phenylmethyl portion. (4S)-3-[(2S,4S)-4-Azido-2-(1-Methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-2-Oxazolidinone also contains various functional groups such as azido, oxo, and methyl, indicating its potential for diverse reactions. The "S" in its chemical name signifies the configuration of the chiral centers in the molecule, suggesting that it may exist in multiple stereoisomeric forms. The extensive structure of this compound implies a highly specific synthesis process, and its uses may be specialized, likely within certain chemical or pharmaceutical applications. Further research would be required to explore its exact properties, reactivity, and potential applications.

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  • (4S)-3-[(2S,4S)-4-Azido-2-(1-Methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-2-Oxazolidinone

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  • (4S)-3-[(2S,4S)-4-Azido-2-(1-Methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-2-Oxazolidinone

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  • (4S)-3-[(2S,4S)-4-AZIDO-2-ISOPROPYL-4-[(2S,4S)-4-ISOPROPYL-5-OXO-TETRAHYDROFURAN-2-YL]BUTANOYL]-4-BENZYL-OXAZOLIDIN-2-ONE

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  • (4S)-3-[(2S,4S)-4-Azido-2-(1-Methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-2-Oxazolidinone

    Cas No: 173154-01-3

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  • 173154-01-3 Structure
  • Basic information

    1. Product Name: (4S)-3-[(2S,4S)-4-Azido-2-(1-Methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-2-Oxazolidinone
    2. Synonyms: (4S)-3-[(2S,4S)-4-Azido-2-(1-Methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-2-Oxazolidinone;2-Oxazolidinone, 3-[4-azido-2-(1-Methylethyl)-1-oxo-4-[tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-, [2S-[2[1(R*),2R*,4R*],4]]-;3-[4-azido-2-(1-Methylethyl)-1-oxo-4-[tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-, [2S-[2[1(R*),2R*,4R*],4]]-2-oxazolidinone;(4S)-3-[(2S,4S)-4-azido-2-isopropyl-4-[(2S,4S)-4-isopropyl-5-oxo-tetrahydrofuran-2-yl]butanoyl]-4-benzyl-oxazolidin-2-one;(4S)-3-[(2S,4S)-4-azido-4-[(2S,4S)-5-oxo-4-propan-2-yloxolan-2-yl]-2-propan-2-ylbutanoyl]-4-benzyl-1,3-oxazolidin-2-one
    3. CAS NO:173154-01-3
    4. Molecular Formula: C24H32N4O5
    5. Molecular Weight: 457
    6. EINECS: 1312995-182-4
    7. Product Categories: N/A
    8. Mol File: 173154-01-3.mol
  • Chemical Properties

    1. Melting Point: 105℃
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (4S)-3-[(2S,4S)-4-Azido-2-(1-Methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-2-Oxazolidinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S)-3-[(2S,4S)-4-Azido-2-(1-Methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-2-Oxazolidinone(173154-01-3)
    11. EPA Substance Registry System: (4S)-3-[(2S,4S)-4-Azido-2-(1-Methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-2-Oxazolidinone(173154-01-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 173154-01-3(Hazardous Substances Data)

173154-01-3 Usage

Uses

Used in Chemical Synthesis:
(4S)-3-[(2S,4S)-4-Azido-2-(1-Methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-2-Oxazolidinone is used as a key intermediate in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. Its unique structure and functional groups allow for targeted reactions and the creation of novel compounds with potential therapeutic applications.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (4S)-3-[(2S,4S)-4-Azido-2-(1-Methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-2-Oxazolidinone is used as a starting material for the development of new drugs. Its structural complexity and the presence of various functional groups make it a promising candidate for the creation of innovative therapeutic agents, potentially targeting a wide range of diseases and conditions.
Used in Research and Development:
(4S)-3-[(2S,4S)-4-Azido-2-(1-Methylethyl)-1-oxo-4-[(2S,4S)-tetrahydro-4-(1-Methylethyl)-5-oxo-2-furanyl]butyl]-4-(phenylMethyl)-2-Oxazolidinone is utilized in research settings to study its chemical properties, reactivity, and potential interactions with other molecules. This information can be crucial for understanding its behavior in various chemical and biological systems, as well as for identifying new applications and uses in different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 173154-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,1,5 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 173154-01:
(8*1)+(7*7)+(6*3)+(5*1)+(4*5)+(3*4)+(2*0)+(1*1)=113
113 % 10 = 3
So 173154-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C24H32N4O5/c1-14(2)18(11-20(26-27-25)21-12-19(15(3)4)23(30)33-21)22(29)28-17(13-32-24(28)31)10-16-8-6-5-7-9-16/h5-9,14-15,17-21H,10-13H2,1-4H3/t17-,18-,19-,20-,21-/m0/s1

173154-01-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S)-3-[(2S,4S)-4-azido-4-[(2S,4S)-5-oxo-4-propan-2-yloxolan-2-yl]-2-propan-2-ylbutanoyl]-4-benzyl-1,3-oxazolidin-2-one

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:173154-01-3 SDS

173154-01-3Relevant articles and documents

1,8-dioxo -4,5-epoxy composition and method of making the same

-

, (2016/10/08)

The invention relates to 1,8-dicarbonyl-4,5-epoxy compound and a preparation method thereof. The structure formula of the 1,8-dicarbonyl-4,5-epoxy compound is shown in the formula I, and the compound I is further opened and closed by azide substitution. A critical midbody azide lactone compound of aliskiren can be obtained at high selectivity and high yield.

A Facile, Six-Step Process for the Synthesis of (3 S,5 S)-3-Isopropyl-5-((2 S,4 S)-4-isopropyl-5-oxo-tetrahydrofuran-2-yl)-2-oxopyrrolidine-1-carboxylic Acid tert -Butyl Ester, the Key Synthetic Intermediate of Aliskiren

Pan, Xianhua,Xu, Siyao,Huang, Rui,Yu, Wansheng,Liu, Feng

, p. 611 - 617 (2015/06/30)

A facile, six-step process for the synthesis of (3S,5S)-3-isopropyl-5-((2S,4S)-4-isopropyl-5-oxotetrahydro- furan-2-yl)-2-oxopyrrolidine-1-carboxylic acid tert-butyl ester from (S)-4-benzyloxazolidin-2-one 2 in an overall 50% yield is reported. The key transformations include: a highly efficient diastereoselective epoxidation, Lewis acid-catalyzed ring-opening with bromide, an SN2 reaction using NaN3, and a tandem reduction-cyclization reaction.

METHODS OF TREATING ALZHEIMER'S DISEASE USING ARYL ALKANOIC ACID AMIDES

-

Page 189, (2010/02/05)

Disclosed are methods for treating Alzheimer’s disease, and other diseases, and/or inhibiting beta-secretase enzyme, and/or inhibiting deposition of A beta peptide in a mammal, by use of compounds of formula 1 (1) wherein the variables R1-R8 and X are defined herein.

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