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CAS

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514206-08-7

(-)-(1S,4R)-4-(nitromethyl)-2-cyclopenten-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 514206-08-7 Structure

  • Basic information

    1. Product Name: (-)-(1S,4R)-4-(nitromethyl)-2-cyclopenten-1-ol
    2. Synonyms:
    3. CAS NO:514206-08-7
    4. Molecular Formula:
    5. Molecular Weight: 143.142
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 514206-08-7.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,4R)-4-(nitromethyl)-2-cyclopenten-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-(1S,4R)-4-(nitromethyl)-2-cyclopenten-1-ol(514206-08-7)
    11. EPA Substance Registry System: (-)-(1S,4R)-4-(nitromethyl)-2-cyclopenten-1-ol(514206-08-7)

  • 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: 514206-08-7(Hazardous Substances Data)

514206-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 514206-08-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,4,2,0 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 514206-08:
(8*5)+(7*1)+(6*4)+(5*2)+(4*0)+(3*6)+(2*0)+(1*8)=107
107 % 10 = 7
So 514206-08-7 is a valid CAS Registry Number.

514206-08-7Relevant articles and documents

A flexible synthesis of carbanucleosides and 5′-nor-1′-homo carbanucleosides from a common precursor

Rajappan, Vasathakumar P,Yin, Xueqiang,Schneller, Stewart W

, p. 9889 - 9895 (2002)

Enzymatic resolution of (±)-1-acetoxy-4-(nitromethyl)-2-cyclopentene (4) provides entry into a facile 10-step route to carbanucleosides and a practical 7-step procedure to 5′-nor-1′-homo carbanucleosides. These routes are illustrated for adenine derivatives but they are adaptable to any heterocyclic base.

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