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CAS

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1378032-34-8

3-(4-(benzyloxy)-3-methoxyphenethyl)-5-pentyl-4,5-dihydroisoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1378032-34-8 Structure

  • Basic information

    1. Product Name: 3-(4-(benzyloxy)-3-methoxyphenethyl)-5-pentyl-4,5-dihydroisoxazole
    2. Synonyms: 3-(4-(benzyloxy)-3-methoxyphenethyl)-5-pentyl-4,5-dihydroisoxazole
    3. CAS NO:1378032-34-8
    4. Molecular Formula:
    5. Molecular Weight: 381.515
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1378032-34-8.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: 3-(4-(benzyloxy)-3-methoxyphenethyl)-5-pentyl-4,5-dihydroisoxazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-(benzyloxy)-3-methoxyphenethyl)-5-pentyl-4,5-dihydroisoxazole(1378032-34-8)
    11. EPA Substance Registry System: 3-(4-(benzyloxy)-3-methoxyphenethyl)-5-pentyl-4,5-dihydroisoxazole(1378032-34-8)

  • 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: 1378032-34-8(Hazardous Substances Data)

1378032-34-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1378032-34-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,8,0,3 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1378032-34:
(9*1)+(8*3)+(7*7)+(6*8)+(5*0)+(4*3)+(3*2)+(2*3)+(1*4)=158
158 % 10 = 8
So 1378032-34-8 is a valid CAS Registry Number.

1378032-34-8Relevant articles and documents

New scalable and eco-friendly synthesis of gingerols

Vijendra Kumar,Srinivas,Bettadaiah

, p. 2993 - 2995 (2012/07/31)

Synthesis of 6-gingerol and its congeners 7- and 9-gingerols has been achieved from eugenol by a new scalable and eco-friendly protocol. The key steps are functionalization of eugenol to the nitro compound and its reaction under optimized condition with terminal alkenes to afford intermediate isoxazolines. The latter on catalytic hydrogenation in presence of Raney nickel afford corresponding gingerols in good yields.

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