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70240-41-4

Isohexyltriphenylphosphonium Bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 70240-41-4 Structure

  • Basic information

    1. Product Name: Isohexyltriphenylphosphonium Bromide
    2. Synonyms: Isohexyltriphenylphosphonium Bromide;(4-Methylpentyl)triphenylphosphoniuM BroMide;(4-Methylpentyl)triphenyl-phosphoniuM BroMide
    3. CAS NO:70240-41-4
    4. Molecular Formula: Br*C24H28P
    5. Molecular Weight: 427.356881
    6. EINECS: N/A
    7. Product Categories: Aromatics;Wittig Reagents
    8. Mol File: 70240-41-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Isohexyltriphenylphosphonium Bromide(CAS DataBase Reference)
    10. NIST Chemistry Reference: Isohexyltriphenylphosphonium Bromide(70240-41-4)
    11. EPA Substance Registry System: Isohexyltriphenylphosphonium Bromide(70240-41-4)

  • 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: 70240-41-4(Hazardous Substances Data)

70240-41-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70240-41-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,2,4 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 70240-41:
(7*7)+(6*0)+(5*2)+(4*4)+(3*0)+(2*4)+(1*1)=84
84 % 10 = 4
So 70240-41-4 is a valid CAS Registry Number.

70240-41-4Relevant articles and documents

SUBSTITUTED ARYLCYCLOPROPYLACETAMIDES AS GLUCOKINASE ACTIVATORS

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Page 39, (2008/06/13)

According to the present invention there is provided a compounds of formula (I): and pharmaceutically acceptable salts thereof.

Studies related to fatty acid desaturation. Part I: Preparation of methyl-substituted nonanols, nonyl bromides and total synthesis of new branched oleic acids

Genard, S.,Patin, H.

, p. 397 - 406 (2007/10/02)

Convenient pathways for the synthesis of seven structurally defined isomers of methyl-nonanols and methyl-nonylbromides are described.These synthons are used to perform Wittig reactions between convenient phosphoranes and aldehydes in order to obtain seven new octadecenoic acids bearing a methyl grouping on carbons 11 to 17. branched nonan-1-ols / branched 1-nonylbromides / Wittig reactions / methyl 9-bromononanoate / methyl 8-formyloctanoate / methyl 11 or 17-methyloctadec-9-enoates

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