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143669-35-6

2-bromo-1,1-dimethoxynonadecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 143669-35-6 Structure

  • Basic information

    1. Product Name: 2-bromo-1,1-dimethoxynonadecane
    2. Synonyms: 2-bromo-1,1-dimethoxynonadecane
    3. CAS NO:143669-35-6
    4. Molecular Formula:
    5. Molecular Weight: 407.475
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 143669-35-6.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: 2-bromo-1,1-dimethoxynonadecane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-bromo-1,1-dimethoxynonadecane(143669-35-6)
    11. EPA Substance Registry System: 2-bromo-1,1-dimethoxynonadecane(143669-35-6)

  • 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: 143669-35-6(Hazardous Substances Data)

143669-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143669-35-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,6,6 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 143669-35:
(8*1)+(7*4)+(6*3)+(5*6)+(4*6)+(3*9)+(2*3)+(1*5)=146
146 % 10 = 6
So 143669-35-6 is a valid CAS Registry Number.

143669-35-6Relevant articles and documents

Syntheses of All Four Stereoisomers Which Are Conformationally Constrained 1,4-Dioxanyl Analogs of the Antineoplastic Ether Lipid ET-18-OCH3

Duclos, Richard I.,Makriyannis, Alexandros

, p. 6156 - 6163 (1992)

The syntheses of each of the four nearly optically pure stereoisomers of oxy>phosphocholine (2,3,2',3') were performed by two parallel divergent sequences.Phosphocholines 2 and 3 were prepared via the corresponding 5-heptadecyl-2-(hydroxymethyl)-1,4-dioxanes 21 and 23, respectively, from the completely regiospecific mixed-hydride reductions of (1R,4S,5S)-4-heptadecyl-3,6,8-trioxabicyclooctane (19) and (1R,4R,5S)-4-heptadecyl-3,6,8-trioxabicyclooctane (20), respectively.The two 4-heptadecyl-3,6,8-trioxabicyclooctanes 19 and 20 were the two separable products from an intramolecular cyclization reaction.By a parallel divergent sequence from the enantiomeric starting material, 3-O-benzyl-sn-glycerol (16'), the other two diastereomeric oxy>phosphocholines 2' and 3' were prepared.These four monocyclic oxy>phosphocholines (2,3,2',3') are conformationally constrained analogs of the antineoplastic and immunomodulatory ether lipid rac-2-O-methyl-1-O-octadecylglycero-3-phosphocholine (rac-1) (rac-ET-18-OCH3, rac-Edelfosine).

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