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CAS

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951793-24-1

1-bromomethyl-2-ethynyl-2-tert-butyldimethylsilyloxymethyl-1-phenylselenylcyclopropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 951793-24-1 Structure

  • Basic information

    1. Product Name: 1-bromomethyl-2-ethynyl-2-tert-butyldimethylsilyloxymethyl-1-phenylselenylcyclopropane
    2. Synonyms: 1-bromomethyl-2-ethynyl-2-tert-butyldimethylsilyloxymethyl-1-phenylselenylcyclopropane
    3. CAS NO:951793-24-1
    4. Molecular Formula:
    5. Molecular Weight: 458.372
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 951793-24-1.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: 1-bromomethyl-2-ethynyl-2-tert-butyldimethylsilyloxymethyl-1-phenylselenylcyclopropane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-bromomethyl-2-ethynyl-2-tert-butyldimethylsilyloxymethyl-1-phenylselenylcyclopropane(951793-24-1)
    11. EPA Substance Registry System: 1-bromomethyl-2-ethynyl-2-tert-butyldimethylsilyloxymethyl-1-phenylselenylcyclopropane(951793-24-1)

  • 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: 951793-24-1(Hazardous Substances Data)

951793-24-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 951793-24-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,7,9 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 951793-24:
(8*9)+(7*5)+(6*1)+(5*7)+(4*9)+(3*3)+(2*2)+(1*4)=201
201 % 10 = 1
So 951793-24-1 is a valid CAS Registry Number.

951793-24-1Relevant articles and documents

Methylene-2-ethynylcyclopropanes: synthesis and biological activity of (Z)- and (E)-9-{[2-ethynyl-2-(hydroxymethyl)cyclopropylidene]methyl}adenine and -guanine

Zhou, Shaoman,Prichard, Mark N.,Zemlicka, Jiri

, p. 9406 - 9412 (2008/02/11)

Synthesis of methylene-2-ethynylcyclopropane analogues of nucleosides 12a, 12b, 13a, and 13b is described. Ethyl methylenecyclopropane carboxylate 14 was hydroxymethylated to give alcohol 15, which was reduced to diol 16. Selective protection with tert-bu

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