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88454-84-6

(2R,3R)-N,N,N',N'-Tetramethyl-2,3-bis<2-<2-(benzyloxy)ethoxy>ethyl>tataramide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 88454-84-6 Structure

  • Basic information

    1. Product Name: (2R,3R)-N,N,N',N'-Tetramethyl-2,3-bis<2-<2-(benzyloxy)ethoxy>ethyl>tataramide
    2. Synonyms:
    3. CAS NO:88454-84-6
    4. Molecular Formula:
    5. Molecular Weight: 560.688
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 88454-84-6.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: (2R,3R)-N,N,N',N'-Tetramethyl-2,3-bis<2-<2-(benzyloxy)ethoxy>ethyl>tataramide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3R)-N,N,N',N'-Tetramethyl-2,3-bis<2-<2-(benzyloxy)ethoxy>ethyl>tataramide(88454-84-6)
    11. EPA Substance Registry System: (2R,3R)-N,N,N',N'-Tetramethyl-2,3-bis<2-<2-(benzyloxy)ethoxy>ethyl>tataramide(88454-84-6)

  • 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: 88454-84-6(Hazardous Substances Data)

88454-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88454-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,5 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88454-84:
(7*8)+(6*8)+(5*4)+(4*5)+(3*4)+(2*8)+(1*4)=176
176 % 10 = 6
So 88454-84-6 is a valid CAS Registry Number.

88454-84-6Downstream Products

88454-84-6Relevant articles and documents

Synthesis of Lipophilic 18-Crown-6 Diacids for the Membrane Transport of Alkaline-Earth Cations

Fyles, Thomas M.,McGavin, Cynthia A.,Whitfield, Dennis M.

, p. 753 - 761 (2007/10/02)

The synthesis of three different types of lipophilic 18-crown-6 diacids is described.A didecyl crown ether 2,3-diacid (1) was prepared as a minor product from a diiodide precursor (12) and threo-11,12-docosanediol by thallous ethoxide cyclization.The major nonpolymeric products resulted from elimination followed by cyclization to give 15-crown-5-derivatives.A crown ether 11,12-diamide 2,3-diacid (4) was prepared by a similar route involving cyclization of a benzyl protected precursor (26) and N,N,N',N'-tetramethyltartaramide (9).Isomeric syn and anti 2,11(12)-diamide 3,12(11)-diacid derivatives 6 and 7 were prepared from the known crown ether bisanhydride 8 and alkylamines.The product mixture was separated by chromatography, and the isomers were identified by comparison of acidity and stability constants for complexation with those of closely related syn/anti crown ether acids.

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