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CAS

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1401624-03-0

(R)-3-[(benzyloxy)methyl]-3-hydroxypyridine-2,6(1H,3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1401624-03-0 Structure

  • Basic information

    1. Product Name: (R)-3-[(benzyloxy)methyl]-3-hydroxypyridine-2,6(1H,3H)-dione
    2. Synonyms:
    3. CAS NO:1401624-03-0
    4. Molecular Formula:
    5. Molecular Weight: 247.251
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1401624-03-0.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: (R)-3-[(benzyloxy)methyl]-3-hydroxypyridine-2,6(1H,3H)-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-3-[(benzyloxy)methyl]-3-hydroxypyridine-2,6(1H,3H)-dione(1401624-03-0)
    11. EPA Substance Registry System: (R)-3-[(benzyloxy)methyl]-3-hydroxypyridine-2,6(1H,3H)-dione(1401624-03-0)

  • 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: 1401624-03-0(Hazardous Substances Data)

1401624-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1401624-03-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,6,2 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1401624-03:
(9*1)+(8*4)+(7*0)+(6*1)+(5*6)+(4*2)+(3*4)+(2*0)+(1*3)=100
100 % 10 = 0
So 1401624-03-0 is a valid CAS Registry Number.

1401624-03-0Downstream Products

1401624-03-0Relevant articles and documents

Enantioselectivity in visible light-induced, singlet oxygen [2+4] cycloaddition reactions (type II photooxygenations) of 2-pyridones

Wiegand, Christian,Herdtweck, Eberhardt,Bach, Thorsten

supporting information, p. 10195 - 10197,3 (2020/08/24)

3-Substituted 2-pyridones were enantioselectively (68-90% ee) converted into the respective 3-hydroxypyridine-2,6-diones by a sequence consisting of a template-mediated type II photooxygenation and an acid-catalysed rearrangement.

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