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CAS

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133281-03-5

5-Heptadecyl-2-benzyloxymethyl-1,3-dioxolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133281-03-5 Structure

  • Basic information

    1. Product Name: 5-Heptadecyl-2-benzyloxymethyl-1,3-dioxolane
    2. Synonyms: 5-Heptadecyl-2-benzyloxymethyl-1,3-dioxolane
    3. CAS NO:133281-03-5
    4. Molecular Formula:
    5. Molecular Weight: 432.687
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133281-03-5.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: 5-Heptadecyl-2-benzyloxymethyl-1,3-dioxolane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Heptadecyl-2-benzyloxymethyl-1,3-dioxolane(133281-03-5)
    11. EPA Substance Registry System: 5-Heptadecyl-2-benzyloxymethyl-1,3-dioxolane(133281-03-5)

  • 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: 133281-03-5(Hazardous Substances Data)

133281-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133281-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,2,8 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133281-03:
(8*1)+(7*3)+(6*3)+(5*2)+(4*8)+(3*1)+(2*0)+(1*3)=95
95 % 10 = 5
So 133281-03-5 is a valid CAS Registry Number.

133281-03-5Relevant articles and documents

Disubstituted tetrahydrofurans and dioxolanes as PAF antagonists

Bartroli,Carceller,Merlos,Garcia-Rafanell,Forn

, p. 373 - 386 (2007/10/02)

A new series of disubstituted tetrahydrofuran and dioxolane derivatives were prepared and evaluated for their PAF antagonist activity in the PAF-induced in vitro platelet-aggregation and in vivo hypotension tests. Several of these compounds exhibited more potent activity than the structurally related 2-[N-acetyl-N-[[[[2-methoxy-3-[(octadecylcarbamoyl)oxy]propoxy] carbonyl]amino]methyl]-1-ethylpyridinium chloride (CV-6209, 3) in the in vitro assay, whereas all showed less potency in the in vivo test. The role of both the substituent nature and the placement and number of oxygen atoms in the ring are discussed. A qualitative SAR study was carried out on these nuclei.

New 1,3-dioxolane-2-yl derivatives of 2-picolylamine

-

, (2008/06/13)

The present invention relates to new 1,3-dioxolan-2-yl derivatives of 2-picolylamine having the formula (I): wherein:, R1 represents an alkyl radical; R2 represents hydrogen, or a C(=O)R4 group, wherein R4 repre

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