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(E)-But-2-enoic acid ((S)-2-hydroxy-tetrahydro-pyran-3-yl)-(4-methoxy-benzyl)-amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 489432-92-0 Structure
  • Basic information

    1. Product Name: (E)-But-2-enoic acid ((S)-2-hydroxy-tetrahydro-pyran-3-yl)-(4-methoxy-benzyl)-amide
    2. Synonyms:
    3. CAS NO:489432-92-0
    4. Molecular Formula:
    5. Molecular Weight: 305.374
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 489432-92-0.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: (E)-But-2-enoic acid ((S)-2-hydroxy-tetrahydro-pyran-3-yl)-(4-methoxy-benzyl)-amide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-But-2-enoic acid ((S)-2-hydroxy-tetrahydro-pyran-3-yl)-(4-methoxy-benzyl)-amide(489432-92-0)
    11. EPA Substance Registry System: (E)-But-2-enoic acid ((S)-2-hydroxy-tetrahydro-pyran-3-yl)-(4-methoxy-benzyl)-amide(489432-92-0)
  • 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: 489432-92-0(Hazardous Substances Data)

489432-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 489432-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,9,4,3 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 489432-92:
(8*4)+(7*8)+(6*9)+(5*4)+(4*3)+(3*2)+(2*9)+(1*2)=200
200 % 10 = 0
So 489432-92-0 is a valid CAS Registry Number.

489432-92-0Downstream Products

489432-92-0Relevant articles and documents

TBAT-mediated nitrone formation of ω-mesyloxy-O-tert-butyldiphenylsilyloximes: Facile synthesis of cyclic nitrones from hemiacetals

Tamura, Osamu,Toyao, Atsushi,Ishibashi, Hiroyuki

, p. 1344 - 1346 (2007/10/03)

Chiral and cyclic nitrones were synthesized by TBAT-mediated desilylative cyclization of ω-mesyloxy-O-tert-butyl-diphenylsilyloximes, readily prepared from sugar derivatives by a consecutive treatment with O-tert-butyldiphenylsilylhydroxylamine and with m

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