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CAS

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118304-54-4

tert-butyldimethylsilyl Δ13-(Z)-retinyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 118304-54-4 Structure

  • Basic information

    1. Product Name: tert-butyldimethylsilyl Δ13-(Z)-retinyl ether
    2. Synonyms: tert-butyldimethylsilyl Δ13-(Z)-retinyl ether
    3. CAS NO:118304-54-4
    4. Molecular Formula:
    5. Molecular Weight: 400.72
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 118304-54-4.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: tert-butyldimethylsilyl Δ13-(Z)-retinyl ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyldimethylsilyl Δ13-(Z)-retinyl ether(118304-54-4)
    11. EPA Substance Registry System: tert-butyldimethylsilyl Δ13-(Z)-retinyl ether(118304-54-4)

  • 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: 118304-54-4(Hazardous Substances Data)

118304-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118304-54-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,0 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 118304-54:
(8*1)+(7*1)+(6*8)+(5*3)+(4*0)+(3*4)+(2*5)+(1*4)=104
104 % 10 = 4
So 118304-54-4 is a valid CAS Registry Number.

118304-54-4Downstream Products

118304-54-4Relevant articles and documents

The simultaneous in-situ generation of aldehydes and phosphorus ylides: A convenient multi-step one-pot olefination protocol

Wang, Qian,Wei, Heng-Xu,Schlosser, Manfred

, p. 3263 - 3268 (2007/10/03)

The lithium α-(dimethylamino)alkoxides resulting from the nucleophilic addition of an organolithium reagent to N,N-dimethylformamide are basic enough to deprotonate alkyltriphenylphosphonium salts suspended in tetrahydrofuran. The aldehydes liberated by t

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