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(3R,2S)-3-propyloxirane-2-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 608520-05-4 Structure
  • Basic information

    1. Product Name: (3R,2S)-3-propyloxirane-2-carboxylic acid
    2. Synonyms: (3R,2S)-3-propyloxirane-2-carboxylic acid
    3. CAS NO:608520-05-4
    4. Molecular Formula:
    5. Molecular Weight: 130.144
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 608520-05-4.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: (3R,2S)-3-propyloxirane-2-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R,2S)-3-propyloxirane-2-carboxylic acid(608520-05-4)
    11. EPA Substance Registry System: (3R,2S)-3-propyloxirane-2-carboxylic acid(608520-05-4)
  • 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: 608520-05-4(Hazardous Substances Data)

608520-05-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 608520-05-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,8,5,2 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 608520-05:
(8*6)+(7*0)+(6*8)+(5*5)+(4*2)+(3*0)+(2*0)+(1*5)=134
134 % 10 = 4
So 608520-05-4 is a valid CAS Registry Number.

608520-05-4Upstream product

608520-05-4Relevant articles and documents

Solid-Phase Total Synthesis of Dehydrotryptophan-Bearing Cyclic Peptides Tunicyclin B, Sclerotide A, CDA3a, and CDA4a using a Protected β-Hydroxytryptophan Building Block

Diamandas, Matthew,Moreira, Ryan,Taylor, Scott D.

, p. 3048 - 3052 (2021)

A new approach to the synthesis of Z-dehydrotryptophan (ΔTrp) peptides is described. This approach uses Fmoc-β-HOTrp(Boc)(TBS)-OH as a building block, which is readily prepared in high yield and incorporated into peptides using solid-phase Fmoc chemistry. The tert-butyldimethylsilyl-protected indolic alcohol is eliminated during global deprotection/resin cleavage to give ΔTrp peptides exclusively as the thermodynamically favored Z isomer. This approach was applied to the solid-phase synthesis of tunicyclin B, sclerotide A, CDA3a, and CDA4a.

SYNTHESIS OF AN INTERMEDIATE OF AN ANTIVIRAL COMPOUND

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Paragraph 0107; 0108, (2014/06/11)

Process for the preparation of a cyclopropylamide compound which is useful as a structural unit in a process for the preparation of a viral protease inhibitor.

Synthesis of an intermediate of an antiviral compound

-

Paragraph 0092-0093, (2014/06/24)

Process for the preparation of a cyclopropylamide compound (II) which is useful as a structural unit in a process for the preparation of a viral protease inhibitor.

First one-pot copper-catalyzed synthesis of α-hydroxy-β-amino acids in water. A new protocol for preparation of optically active norstatines

Fringuelli, Francesco,Pizzo, Ferdinando,Rucci, Mauro,Vaccaro, Luigi

, p. 7041 - 7045 (2007/10/03)

α-Hydroxy-β-amino acids were synthesized with excellent yields for the first time in water and by a simple procedure based on a copper catalytic cycle, which included the recovery and reuse of the catalyst and is possible to realize by using only water as reaction medium.

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