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123719-63-1

2(3H)-Benzoxazolone,7a-ethenylhexahydro-,trans-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123719-63-1 Structure

  • Basic information

    1. Product Name: 2(3H)-Benzoxazolone,7a-ethenylhexahydro-,trans-(9CI)
    2. Synonyms: 2(3H)-Benzoxazolone,7a-ethenylhexahydro-,trans-(9CI)
    3. CAS NO:123719-63-1
    4. Molecular Formula: C9H13NO2
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N-BOC
    8. Mol File: 123719-63-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2(3H)-Benzoxazolone,7a-ethenylhexahydro-,trans-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2(3H)-Benzoxazolone,7a-ethenylhexahydro-,trans-(9CI)(123719-63-1)
    11. EPA Substance Registry System: 2(3H)-Benzoxazolone,7a-ethenylhexahydro-,trans-(9CI)(123719-63-1)

  • 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: 123719-63-1(Hazardous Substances Data)

123719-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123719-63-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,7,1 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 123719-63:
(8*1)+(7*2)+(6*3)+(5*7)+(4*1)+(3*9)+(2*6)+(1*3)=121
121 % 10 = 1
So 123719-63-1 is a valid CAS Registry Number.

123719-63-1Downstream Products

123719-63-1Relevant articles and documents

STEREOSELECTIVE SYNTHESIS OF SUBSTITUTED PIPECOLIC ACIDS

Angle, Steven R.,Arnaiz, Damian O.

, p. 515 - 518 (2007/10/02)

The stereoselective synthesis of Δ4,5-pipecolic acid derivatives is described.The key step in the sequence is a sigmatropic rearrangement.

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