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CAS

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1012341-29-5

C18H25NO2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1012341-29-5 Structure

  • Basic information

    1. Product Name: C18H25NO2
    2. Synonyms:
    3. CAS NO:1012341-29-5
    4. Molecular Formula:
    5. Molecular Weight: 287.402
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1012341-29-5.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: C18H25NO2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H25NO2(1012341-29-5)
    11. EPA Substance Registry System: C18H25NO2(1012341-29-5)

  • 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: 1012341-29-5(Hazardous Substances Data)

1012341-29-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1012341-29-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,2,3,4 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1012341-29:
(9*1)+(8*0)+(7*1)+(6*2)+(5*3)+(4*4)+(3*1)+(2*2)+(1*9)=75
75 % 10 = 5
So 1012341-29-5 is a valid CAS Registry Number.

1012341-29-5Upstream product

1012341-29-5Downstream Products

1012341-29-5Relevant articles and documents

Enantioselective synthesis of cis-4-formyl-β-lactams via chiral N-heterocyclic carbene-catalyzed kinetic resolution

Li, Gong-Qiang,Li, Yi,Dai, Li-Xin,You, Shu-Li

, p. 1258 - 1262 (2008)

An efficient synthesis of optically pure cis-4-formyl-β-lactams (up to 99% ee) by a chiral NHC-catalyzed ring expansion reaction has been realized, featuring the ready availability of both the substrate and the catalyst, and the mild reaction conditions. The current method is also suitable for the synthesis of enantioenriched 4-formyl-β-lactams and succinimides containing quaternary carbon centers.

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