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1334334-67-6

(Z)-ethyl 4-(tert-butyldimethylsilyloxy)-2-(hydroxy(phenyl)methyl)but-2-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1334334-67-6 Structure

  • Basic information

    1. Product Name: (Z)-ethyl 4-(tert-butyldimethylsilyloxy)-2-(hydroxy(phenyl)methyl)but-2-enoate
    2. Synonyms: (Z)-ethyl 4-(tert-butyldimethylsilyloxy)-2-(hydroxy(phenyl)methyl)but-2-enoate
    3. CAS NO:1334334-67-6
    4. Molecular Formula:
    5. Molecular Weight: 350.53
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1334334-67-6.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: (Z)-ethyl 4-(tert-butyldimethylsilyloxy)-2-(hydroxy(phenyl)methyl)but-2-enoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-ethyl 4-(tert-butyldimethylsilyloxy)-2-(hydroxy(phenyl)methyl)but-2-enoate(1334334-67-6)
    11. EPA Substance Registry System: (Z)-ethyl 4-(tert-butyldimethylsilyloxy)-2-(hydroxy(phenyl)methyl)but-2-enoate(1334334-67-6)

  • 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: 1334334-67-6(Hazardous Substances Data)

1334334-67-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1334334-67-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,3,3 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1334334-67:
(9*1)+(8*3)+(7*3)+(6*4)+(5*3)+(4*3)+(3*4)+(2*6)+(1*7)=136
136 % 10 = 6
So 1334334-67-6 is a valid CAS Registry Number.

1334334-67-6Relevant articles and documents

Custom synthesis of substituted butenolides, dihydropyranones, and α-E-alkylidenelactones via alkenylalumination

Veeraraghavan Ramachandran,Pratihar, Debarshi,Garner, Garrett,China Raju

, p. 4985 - 4988 (2011/10/08)

Alkenylalumination of aldehydes with [α-(ethoxycarbonyl)-β-(t- butyldimethylsilyloxyalkyl)alkenyl]diisobutylaluminum provides the corresponding α-Z-alkylidene-β′-hydroxy esters, which upon protection and treatment with trifluoroacetic acid lactonizes to f

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