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CAS

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73821-96-2

(2S)-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-cyclohexyl ester is a complex organic molecule with a pentanedioic acid core, featuring a benzyl ester and a cyclohexyl ester, as well as a tert-butoxycarbonylamino group. This derivative of pentanedioic acid has multiple ester groups and a protective group for the amine function, which may be useful in various applications in organic synthesis and chemical research.

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  • 73821-96-2 Structure

  • Basic information

    1. Product Name: (2S)-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-cyclohexyl ester
    2. Synonyms: (2S)-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-cyclohexyl ester
    3. CAS NO:73821-96-2
    4. Molecular Formula:
    5. Molecular Weight: 419.518
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73821-96-2.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: (2S)-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-cyclohexyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S)-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-cyclohexyl ester(73821-96-2)
    11. EPA Substance Registry System: (2S)-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-cyclohexyl ester(73821-96-2)

  • 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: 73821-96-2(Hazardous Substances Data)

73821-96-2 Usage

Uses

Used in Organic Synthesis:
(2S)-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-cyclohexyl ester is used as an intermediate in organic synthesis for its unique combination of functional groups, which can be further modified or used to construct more complex molecules.
Used in Chemical Research:
In the field of chemical research, (2S)-tert-butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-cyclohexyl ester serves as a model compound to study the reactivity and properties of esters and protected amines, potentially leading to advancements in synthetic methodologies and understanding of molecular interactions.

Check Digit Verification of cas no

The CAS Registry Mumber 73821-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,2 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73821-96:
(7*7)+(6*3)+(5*8)+(4*2)+(3*1)+(2*9)+(1*6)=142
142 % 10 = 2
So 73821-96-2 is a valid CAS Registry Number.

73821-96-2Downstream Products

73821-96-2Relevant articles and documents

Application of a unique automated synthesis system for solution-phase peptide synthesis

Sugawara,Kobayashi,Okamoto,Kitada,Fujino

, p. 1272 - 1280 (1995)

An automated synthesis system, which is suitable for repetitive syntheses using similar reaction procedures, was used to synthesize systematically a library of all possible dipeptides (25) and tripeptides (125) from 5 protected amino acids. The apparatus has also been applied to the automated synthesis of 10 fragment tripeptide derivatives that are constituents of the hormone PACAP-27. The measured molecular optical rotation values of the library of 125 tripeptides were found to correlate well with calculated values obtained by summation of the molecular optical rotation values for the constituent amino acids.

Inhibition of P-glycoprotein-mediated multidrug efflux by aminomethylene and ketomethylene analogs of reversins

Koubeissi, Ali,Raad, Imad,Ettouati, Laurent,Guilet, David,Dumontet, Charles,Paris, Joelle

, p. 5700 - 5703 (2007/10/03)

Several aminomethylene analogs and a ketomethylene analog of reversins were synthesized in order to evaluate their ability to inhibit P-glycoprotein-mediated drug efflux in K562/R7 human leukemic cells overexpressing P-glycoprotein. These analogs retained

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