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CAS

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1436434-08-0

(E)-1-benzyl-3-(1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-2-enyl)urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1436434-08-0 Structure

  • Basic information

    1. Product Name: (E)-1-benzyl-3-(1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-2-enyl)urea
    2. Synonyms:
    3. CAS NO:1436434-08-0
    4. Molecular Formula:
    5. Molecular Weight: 330.235
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1436434-08-0.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: (E)-1-benzyl-3-(1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-2-enyl)urea(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-1-benzyl-3-(1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-2-enyl)urea(1436434-08-0)
    11. EPA Substance Registry System: (E)-1-benzyl-3-(1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-2-enyl)urea(1436434-08-0)

  • 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: 1436434-08-0(Hazardous Substances Data)

1436434-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1436434-08-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,6,4,3 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1436434-08:
(9*1)+(8*4)+(7*3)+(6*6)+(5*4)+(4*3)+(3*4)+(2*0)+(1*8)=150
150 % 10 = 0
So 1436434-08-0 is a valid CAS Registry Number.

1436434-08-0Downstream Products

1436434-08-0Relevant articles and documents

[3,3]-Sigmatropic rearrangement of boronated allylcyanates: A new route to α-aminoboronate derivatives and trisubstituted tetrahydrofurans

Touchet, Sabrina,Macé, Aurélie,Roisnel, Thierry,Carreaux, Fran?ois,Bouillon, Alexandre,Carboni, Bertrand

, p. 2712 - 2715 (2013)

[3,3]-Sigmatropic cyanate-isocyanate rearrangement provides a powerful tool for the preparation of α-isocyanato allylboronic esters, which can be further trapped with a variety of nucleophiles. Hydrogenation gave the corresponding α-aminoboronates derivatives while addition of aldehydes afforded homoallylic alcohols, (tetrahydrofuran-2-yl)carbamate, ether, or urea derivatives.

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