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1031282-20-8

C24H21NO4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1031282-20-8 Structure

  • Basic information

    1. Product Name: C24H21NO4
    2. Synonyms: C24H21NO4
    3. CAS NO:1031282-20-8
    4. Molecular Formula:
    5. Molecular Weight: 387.435
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1031282-20-8.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: C24H21NO4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C24H21NO4(1031282-20-8)
    11. EPA Substance Registry System: C24H21NO4(1031282-20-8)

  • 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: 1031282-20-8(Hazardous Substances Data)

1031282-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1031282-20-8 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 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1031282-20:
(9*1)+(8*0)+(7*3)+(6*1)+(5*2)+(4*8)+(3*2)+(2*2)+(1*0)=88
88 % 10 = 8
So 1031282-20-8 is a valid CAS Registry Number.

1031282-20-8Upstream product

1031282-20-8Downstream Products

1031282-20-8Relevant articles and documents

Synthesis of a new class of C2-symmetrical biheteroaryls by ammonium cerium(IV) nitrate mediated dimerization of 2-(furan-3-yl)pyrroles

Alcaide, Benito,Almendros, Pedro,Carrascosa, Rocio,Rosario Torres

supporting information; experimental part, p. 823 - 826 (2010/04/02)

Polyfunctionalized 2-(furan-2-yl)pyrroles and 2-(furan-3-yl)pyrroles derived from 2-azetidinone-tethered alienes by two independent cerium(IV)-mediated single-electron oxidations provided a (4-oxopent-2-enoyl) pyrrole and 3,3′-bis(pyrrol-2-yl)-2, 2′-bifurans, respectively. Access to the oxidation precursors was achieved by regiocontrolled cyclization of β-allenamine intermediates derived from selective β-lactam nucleus breakage of 2-azetidinone-tethered allenols.

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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