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CAS

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636603-06-0

4-(tert-butyl-diphenyl-silanyloxymethyl)-3-(3-oxo-butyl)-pent-4-enal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 636603-06-0 Structure

  • Basic information

    1. Product Name: 4-(tert-butyl-diphenyl-silanyloxymethyl)-3-(3-oxo-butyl)-pent-4-enal
    2. Synonyms:
    3. CAS NO:636603-06-0
    4. Molecular Formula:
    5. Molecular Weight: 422.64
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 636603-06-0.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: 4-(tert-butyl-diphenyl-silanyloxymethyl)-3-(3-oxo-butyl)-pent-4-enal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(tert-butyl-diphenyl-silanyloxymethyl)-3-(3-oxo-butyl)-pent-4-enal(636603-06-0)
    11. EPA Substance Registry System: 4-(tert-butyl-diphenyl-silanyloxymethyl)-3-(3-oxo-butyl)-pent-4-enal(636603-06-0)

  • 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: 636603-06-0(Hazardous Substances Data)

636603-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 636603-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,6,6,0 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 636603-06:
(8*6)+(7*3)+(6*6)+(5*6)+(4*0)+(3*3)+(2*0)+(1*6)=150
150 % 10 = 0
So 636603-06-0 is a valid CAS Registry Number.

636603-06-0Relevant articles and documents

Asymmetric Total Synthesis of Pseudoplexaurol and 14-Deoxycrassin, two Antitumor Marine Cembrane Diterpenoids

Liu, Zuosheng,Peng, Lizeng,Li, Weidong Z.,Li, Yulin

, p. 1977 - 1980 (2003)

The first asymmetric total synthesis of two naturally occurring antitumor pseudoplexaurol and 14-deoxycrassin were achieved via two convergent synthetic sequences featured a chiral pool protocol to implement C-1 stereogenic center and Ti(0)-mediated cyclization leading to cembrane ring.

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