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CAS

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1428737-98-7

(3R,4R)-4-((4-methoxybenzyl)oxy)-3-methylpentan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1428737-98-7 Structure

  • Basic information

    1. Product Name: (3R,4R)-4-((4-methoxybenzyl)oxy)-3-methylpentan-2-one
    2. Synonyms: (3R,4R)-4-((4-methoxybenzyl)oxy)-3-methylpentan-2-one
    3. CAS NO:1428737-98-7
    4. Molecular Formula:
    5. Molecular Weight: 236.311
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1428737-98-7.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: (3R,4R)-4-((4-methoxybenzyl)oxy)-3-methylpentan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R,4R)-4-((4-methoxybenzyl)oxy)-3-methylpentan-2-one(1428737-98-7)
    11. EPA Substance Registry System: (3R,4R)-4-((4-methoxybenzyl)oxy)-3-methylpentan-2-one(1428737-98-7)

  • 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: 1428737-98-7(Hazardous Substances Data)

1428737-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428737-98-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,7,3 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1428737-98:
(9*1)+(8*4)+(7*2)+(6*8)+(5*7)+(4*3)+(3*7)+(2*9)+(1*8)=197
197 % 10 = 7
So 1428737-98-7 is a valid CAS Registry Number.

1428737-98-7Relevant articles and documents

Synthesis of the C(7)-C(20) fragment of spirotoamides A, B and C

Rossini, Allan F.C.,Dias, Luiz C.

, p. 1567 - 1578 (2019/10/01)

This work describes the preparation of the C(7)-C(20) fragment of spirotoamides A to C in a very elegant fashion, achievement very high levels of stereocontrol. The synthesis has been accomplished by a sequence involving 14 steps (0.36percent overall yiel

Synthesis of the C-1-C-17 fragment of amphidinolides C, C2, C3, and F

Clark, J. Stephen,Yang, Guang,Osnowski, Andrew P.

, p. 1460 - 1463 (2013/06/26)

The C-1-C-17 fragment of amphidinolides C, C2, C3, and F has been constructed from a trans-2,5-disubstituted dihydrofuranone prepared by diastereoselective rearrangement of a free or metal-bound oxonium ylide generated from a metal carbenoid. The dihydrofuranone was converted into an aldehyde corresponding to the C-1-C-8 framework, and this was coupled to the C-9-C-17 unit by nucleophilic addition of a vinylic anion.

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