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1059096-42-2

ethyl (1R,2S)-2-acetylaminocyclopent-3-enecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1059096-42-2 Structure

  • Basic information

    1. Product Name: ethyl (1R,2S)-2-acetylaminocyclopent-3-enecarboxylate
    2. Synonyms:
    3. CAS NO:1059096-42-2
    4. Molecular Formula:
    5. Molecular Weight: 197.234
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1059096-42-2.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: ethyl (1R,2S)-2-acetylaminocyclopent-3-enecarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl (1R,2S)-2-acetylaminocyclopent-3-enecarboxylate(1059096-42-2)
    11. EPA Substance Registry System: ethyl (1R,2S)-2-acetylaminocyclopent-3-enecarboxylate(1059096-42-2)

  • 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: 1059096-42-2(Hazardous Substances Data)

1059096-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1059096-42-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,9,0,9 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1059096-42:
(9*1)+(8*0)+(7*5)+(6*9)+(5*0)+(4*9)+(3*6)+(2*4)+(1*2)=162
162 % 10 = 2
So 1059096-42-2 is a valid CAS Registry Number.

1059096-42-2Upstream product

1059096-42-2Downstream Products

1059096-42-2Relevant articles and documents

Efficient synthesis of hydroxy-substituted cispentacin derivatives

Benedek, Gabriella,Palko, Marta,Weber, Edit,Martinek, Tamas A.,Forro, Eniko,Fueloep, Ferenc

, p. 3724 - 3730 (2008)

Starting from N-protected cis- and trans-2-aminocyclopent-3-enecarboxylic acid derivatives, isomers of 2-amino-3-hydroxycyclopentanecarboxylic acid (8 and 12) were prepared via oxazoline intermediates, whereas the stereoisomeric 2-amino-3,4-dihydroxycyclo

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