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1031281-98-7

C22H23NO4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1031281-98-7 Structure

  • Basic information

    1. Product Name: C22H23NO4
    2. Synonyms: C22H23NO4
    3. CAS NO:1031281-98-7
    4. Molecular Formula:
    5. Molecular Weight: 365.429
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1031281-98-7.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: C22H23NO4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H23NO4(1031281-98-7)
    11. EPA Substance Registry System: C22H23NO4(1031281-98-7)

  • 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: 1031281-98-7(Hazardous Substances Data)

1031281-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1031281-98-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,1,2,8 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1031281-98:
(9*1)+(8*0)+(7*3)+(6*1)+(5*2)+(4*8)+(3*1)+(2*9)+(1*8)=107
107 % 10 = 7
So 1031281-98-7 is a valid CAS Registry Number.

1031281-98-7Upstream product

1031281-98-7Downstream Products

1031281-98-7Relevant articles and documents

New regiocontrolled synthesis of functionalized pyrroles from 2-azetidinone-tethered allenols

Alcaide, Benito,Almendros, Pedro,Carrascosa, Rocio,Redondo, Maria C.

, p. 637 - 643 (2008/12/21)

A new one-pot approach to synthesize densely substituted racemic and enantiopure pyrroles from β-lactams has been developed. The approach relies on the regiocontrolled cyclization of β-allenamine intermediates derived from the ring opening of 2-azetidinon

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