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CAS

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866467-72-3

methyl ({[(4R)-1,3-dibenzyl-5-methoxy-2-oxo-imidazolidin-4-yl]methyl}thio)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 866467-72-3 Structure

  • Basic information

    1. Product Name: methyl ({[(4R)-1,3-dibenzyl-5-methoxy-2-oxo-imidazolidin-4-yl]methyl}thio)acetate
    2. Synonyms: methyl ({[(4R)-1,3-dibenzyl-5-methoxy-2-oxo-imidazolidin-4-yl]methyl}thio)acetate
    3. CAS NO:866467-72-3
    4. Molecular Formula:
    5. Molecular Weight: 414.525
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 866467-72-3.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: methyl ({[(4R)-1,3-dibenzyl-5-methoxy-2-oxo-imidazolidin-4-yl]methyl}thio)acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl ({[(4R)-1,3-dibenzyl-5-methoxy-2-oxo-imidazolidin-4-yl]methyl}thio)acetate(866467-72-3)
    11. EPA Substance Registry System: methyl ({[(4R)-1,3-dibenzyl-5-methoxy-2-oxo-imidazolidin-4-yl]methyl}thio)acetate(866467-72-3)

  • 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: 866467-72-3(Hazardous Substances Data)

866467-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 866467-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,4,6 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 866467-72:
(8*8)+(7*6)+(6*6)+(5*4)+(4*6)+(3*7)+(2*7)+(1*2)=223
223 % 10 = 3
So 866467-72-3 is a valid CAS Registry Number.

866467-72-3Relevant articles and documents

An unusual stereochemical outcome of radical cyclization: Synthesis of (+)-biotin

Chavan, Subhash P.,Chittiboyina, Amar G.,Ramakrishna, Guduru,Tejwani, Rajkumar B.,Ravindranathan,Kamat, Subhash K.,Rai, Beena,Sivadasan, Latha,Balakrishnan, Kamalam,Ramalingam,Deshpande

, p. 9273 - 9280 (2007/10/03)

An enantioselective synthesis of (+)-biotin 1 starting from naturally available cysteine is described. The key steps are the unusual stereochemical outcome of radical cyclization of compound 10 to prepare 5,5-fused system 11, and the introduction of C4-sidechain at C6 in 13 via a Grignard reaction.

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