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CAS

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1374982-10-1

(2S,6S)-benzyl 2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-6-methoxymorpholine-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1374982-10-1 Structure

  • Basic information

    1. Product Name: (2S,6S)-benzyl 2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-6-methoxymorpholine-4-carboxylate
    2. Synonyms:
    3. CAS NO:1374982-10-1
    4. Molecular Formula:
    5. Molecular Weight: 410.426
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1374982-10-1.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: (2S,6S)-benzyl 2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-6-methoxymorpholine-4-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,6S)-benzyl 2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-6-methoxymorpholine-4-carboxylate(1374982-10-1)
    11. EPA Substance Registry System: (2S,6S)-benzyl 2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl]-6-methoxymorpholine-4-carboxylate(1374982-10-1)

  • 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: 1374982-10-1(Hazardous Substances Data)

1374982-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374982-10-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,9,8 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1374982-10:
(9*1)+(8*3)+(7*7)+(6*4)+(5*9)+(4*8)+(3*2)+(2*1)+(1*0)=191
191 % 10 = 1
So 1374982-10-1 is a valid CAS Registry Number.

1374982-10-1Upstream product

1374982-10-1Downstream Products

1374982-10-1Relevant articles and documents

Stereocontrolled access to optically-enriched oxabispidines

Brice, Heloise,Gill, Duncan M.,Goldie, Laura,Keegan, Philip S.,Kerr, William J.,Svensson, Per H.

, p. 4836 - 4838 (2012)

A range of chiral, optically-enriched bicyclic oxabispidines were prepared from (S)-(-)-2,3-epoxypropylphthalimide using an efficient sequence featuring a stereocontrolled intramolecular Mannich reaction as the key transformation.

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