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CAS

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2126144-72-5

(1S,2R)-1-benzyl-2-hydroxy-3-[isobutyl-(4-acetylaminobenzenesulfonyl amino)propyl]carbamic acid tert-butyl ester is a complex organic compound with a unique structure and properties. It consists of a benzyl group attached to a hydroxy and carbamic acid functional group, along with an isobutyl group and an acetylaminobenzenesulfonyl amino group, in the form of a tert-butyl ester.

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  • tert-butyl N-[(2R,3R)-3-hydroxy-4-[N-(2-methylpropyl)-4-acetamidobenzenesulfonamido]-1-phenylbutan-2-yl]carbamate

    Cas No: 2126144-72-5

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  • 2126144-72-5 Structure

  • Basic information

    1. Product Name: (1S,2R)-1-benzyl-2-hydroxy-3-[isobutyl-(4-acetylaminobenzenesulfonyl amino)propyl]carbamic acid tert-butyl ester
    2. Synonyms:
    3. CAS NO:2126144-72-5
    4. Molecular Formula:
    5. Molecular Weight: 533.689
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2126144-72-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (1S,2R)-1-benzyl-2-hydroxy-3-[isobutyl-(4-acetylaminobenzenesulfonyl amino)propyl]carbamic acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S,2R)-1-benzyl-2-hydroxy-3-[isobutyl-(4-acetylaminobenzenesulfonyl amino)propyl]carbamic acid tert-butyl ester(2126144-72-5)
    11. EPA Substance Registry System: (1S,2R)-1-benzyl-2-hydroxy-3-[isobutyl-(4-acetylaminobenzenesulfonyl amino)propyl]carbamic acid tert-butyl ester(2126144-72-5)

  • 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: 2126144-72-5(Hazardous Substances Data)

2126144-72-5 Usage

Uses

Used in Pharmaceutical and Drug Development:
(1S,2R)-1-benzyl-2-hydroxy-3-[isobutyl-(4-acetylaminobenzenesulfonyl amino)propyl]carbamic acid tert-butyl ester is used as a pharmaceutical compound for its potential applications in drug development. Its unique structure and properties make it a promising candidate for the creation of new drugs and therapies.
Used in Chemical Research:
(1S,2R)-1-benzyl-2-hydroxy-3-[isobutyl-(4-acetylaminobenzenesulfonyl amino)propyl]carbamic acid tert-butyl ester is also used as a research compound in chemical research. Its complex structure and properties allow scientists to study and explore its potential applications and interactions with other compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 2126144-72-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,1,2,6,1,4 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2126144-72:
(9*2)+(8*1)+(7*2)+(6*6)+(5*1)+(4*4)+(3*4)+(2*7)+(1*2)=125
125 % 10 = 5
So 2126144-72-5 is a valid CAS Registry Number.

2126144-72-5Downstream Products

2126144-72-5Relevant articles and documents

PROCESS FOR THE PREPARATION OF DARUNAVIR

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, (2016/12/22)

The present invention provides a cost effective and industrially feasible process for preparation of Darunavir (I). Also described is the novel salt of intermediate 4-Amino-N- ((2R,3S)-3-amino-2-hydroxy-4-phenylbutyl)-N-isobutylbenzene sulfonamide acid salt (VIII) and its use in the preparation of Darunavir. Formula (I) and (VII).

PROCESS FOR PREPARATION OF DARUNAVIR

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Paragraph 0171; 172; 0173, (2015/07/27)

Provided are a process for preparation of darunavir or solvates or a pharmaceutically acceptable salt thereof substantially free of bisfuranyl impurities and a process for preparation of amorphous darunavir using the darunavir propionate solvate.

PROCESS FOR THE PREPARATION OF SULFONAMIDES USEFUL AS RETROVIRAL PROTEASE INHIBITORS

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, (2013/03/26)

The present invention relates to a process for the preparation of sulfonamides useful as retroviral protease inhibitors.

Sulfonamide inhibitors of aspartyl protease

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Example 39, (2008/06/13)

The present invention relates to a novel class of sulfonamides which are aspartyl protease inhibitors. In one embodiment, this invention relates to a novel class of HIV aspartyl protease inhibitors characterized by specific structural and physicochemical features. This invention also relates to pharmaceutical compositions comprising these compounds. The compounds and pharmaceutical compositions of this invention are particularly well suited for inhibiting HIV-1 and HIV-2 protease activity and consequently, may be advantageously used as anti-viral agents against the HIV-1 and HIV-2 viruses. This invention also relates to methods for inhibiting the activity of HIV aspartyl protease using the compounds of this invention and methods for screening compounds for anti-HIV activity.

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