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CAS

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153229-38-0

3-Iodo-2,2,4-trimethyl-1-trimethylsilanyloxy-cyclohex-3-enecarbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 153229-38-0 Structure

  • Basic information

    1. Product Name: 3-Iodo-2,2,4-trimethyl-1-trimethylsilanyloxy-cyclohex-3-enecarbaldehyde
    2. Synonyms: 3-Iodo-2,2,4-trimethyl-1-trimethylsilanyloxy-cyclohex-3-enecarbaldehyde
    3. CAS NO:153229-38-0
    4. Molecular Formula:
    5. Molecular Weight: 366.314
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 153229-38-0.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: 3-Iodo-2,2,4-trimethyl-1-trimethylsilanyloxy-cyclohex-3-enecarbaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Iodo-2,2,4-trimethyl-1-trimethylsilanyloxy-cyclohex-3-enecarbaldehyde(153229-38-0)
    11. EPA Substance Registry System: 3-Iodo-2,2,4-trimethyl-1-trimethylsilanyloxy-cyclohex-3-enecarbaldehyde(153229-38-0)

  • 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: 153229-38-0(Hazardous Substances Data)

153229-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153229-38-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,2,2 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 153229-38:
(8*1)+(7*5)+(6*3)+(5*2)+(4*2)+(3*9)+(2*3)+(1*8)=120
120 % 10 = 0
So 153229-38-0 is a valid CAS Registry Number.

153229-38-0Relevant articles and documents

Stereocontrolled syntheses of C-aryl taxanes by intramolecular Heck olefination. Novel instances of diastereofacial guidance by proximal coordination

Young, Wendy B.,Masters, John J.,Danishefsky, Samuel

, p. 5228 - 5234 (2007/10/02)

Stereospecific syntheses of baccatin III constructs bearing an aromatic C-ring (2a and 2b) have been demonstrated. A key step involves the use of an intramolecular Heck olefination reaction to form the C10-C11 bond. Novel stereospeci

A CONCISE SYNTHESIS OF A HIGHLY FUNCTIONALIZED C-ARYL TAXOL ANALOG BY AN INTRAMOLECULAR HECK OLEFINATION REACTION

Masters, John J.,Jung, David K.,Bornmann, William G.,Danishefsky, Samuel J.,Gala, Susan de

, p. 7253 - 7256 (2007/10/02)

A palladium(O) catalyzed intramolecular Heck olefination used to establish the C10-C11 connection in a highly functionalized taxane analog is described.

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