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108717-53-9

phenyl-1 dimethyl-4,8 nonadiene-3,7 ol-2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 108717-53-9 Structure

  • Basic information

    1. Product Name: phenyl-1 dimethyl-4,8 nonadiene-3,7 ol-2
    2. Synonyms:
    3. CAS NO:108717-53-9
    4. Molecular Formula:
    5. Molecular Weight: 244.377
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108717-53-9.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: phenyl-1 dimethyl-4,8 nonadiene-3,7 ol-2(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenyl-1 dimethyl-4,8 nonadiene-3,7 ol-2(108717-53-9)
    11. EPA Substance Registry System: phenyl-1 dimethyl-4,8 nonadiene-3,7 ol-2(108717-53-9)

  • 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: 108717-53-9(Hazardous Substances Data)

108717-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108717-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,1 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 108717-53:
(8*1)+(7*0)+(6*8)+(5*7)+(4*1)+(3*7)+(2*5)+(1*3)=129
129 % 10 = 9
So 108717-53-9 is a valid CAS Registry Number.

108717-53-9Downstream Products

108717-53-9Relevant articles and documents

Le benzyltrimethylsilane, un agent pratique de benzylation

Bennetau, Bernard,Bordeau, Michel,Dunogues, Jacques

, p. 90 - 93 (2007/10/02)

In the presence of Bu4N(1+))*F(1-), benzyltrimethylsilane behaves as a convenient benzylation reagent.In the reaction with non conjugated aldehydes, pehenethylalcohols are obtained in satisfactory yields upon hydrolysis, while the formation of bibenzyl or ortho products are not observed.When the reaction occurs with α,β-unsaturated aldehydes and ketones, only 1,2-addition is observed even in the case of chalcone.

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