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1454711-10-4

1-(4-methoxybenzyloxy)-3-methylbutanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1454711-10-4 Structure

  • Basic information

    1. Product Name: 1-(4-methoxybenzyloxy)-3-methylbutanal
    2. Synonyms: 1-(4-methoxybenzyloxy)-3-methylbutanal
    3. CAS NO:1454711-10-4
    4. Molecular Formula:
    5. Molecular Weight: 222.284
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1454711-10-4.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: 1-(4-methoxybenzyloxy)-3-methylbutanal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-methoxybenzyloxy)-3-methylbutanal(1454711-10-4)
    11. EPA Substance Registry System: 1-(4-methoxybenzyloxy)-3-methylbutanal(1454711-10-4)

  • 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: 1454711-10-4(Hazardous Substances Data)

1454711-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1454711-10-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,4,7,1 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1454711-10:
(9*1)+(8*4)+(7*5)+(6*4)+(5*7)+(4*1)+(3*1)+(2*1)+(1*0)=144
144 % 10 = 4
So 1454711-10-4 is a valid CAS Registry Number.

1454711-10-4Relevant articles and documents

Asymmetric synthesis of the C1-C6 portion of the psymberin using an Evans chiral auxiliary

Pal, Ashutosh,Peng, Zhenghong,Schuber Jr., Paul T.,Bhanu Prasad, Basvoju A.,Bornmann, William G.

, p. 5555 - 5557 (2013)

The C1-C6 region of the potent cytotoxic agent psymberin has been synthesized. The key transformations of the synthesis are an auxiliary-controlled addition of a Sn(II)-glycolate enolate to an aldehyde to yield the anti-aldol product and transforming the

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