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CAS

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389626-36-2

1,2-Cyclopropanedimethanol, 1-[(triphenylmethoxy)methyl]-, (1R,2R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 389626-36-2 Structure

  • Basic information

    1. Product Name: 1,2-Cyclopropanedimethanol, 1-[(triphenylmethoxy)methyl]-, (1R,2R)-
    2. Synonyms:
    3. CAS NO:389626-36-2
    4. Molecular Formula: C25H26O3
    5. Molecular Weight: 374.48
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 389626-36-2.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: 1,2-Cyclopropanedimethanol, 1-[(triphenylmethoxy)methyl]-, (1R,2R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Cyclopropanedimethanol, 1-[(triphenylmethoxy)methyl]-, (1R,2R)-(389626-36-2)
    11. EPA Substance Registry System: 1,2-Cyclopropanedimethanol, 1-[(triphenylmethoxy)methyl]-, (1R,2R)-(389626-36-2)

  • 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: 389626-36-2(Hazardous Substances Data)

389626-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 389626-36-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,6,2 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 389626-36:
(8*3)+(7*8)+(6*9)+(5*6)+(4*2)+(3*6)+(2*3)+(1*6)=202
202 % 10 = 2
So 389626-36-2 is a valid CAS Registry Number.

389626-36-2Relevant articles and documents

Carbocyclic nucleoside precursors by intramolecular cyclopropanation of sugar-derived diazo compounds

Gallos, John K,Massen, Zoe S,Koftis, Theocharis V,Dellios, Constantinos C

, p. 7489 - 7491 (2001)

Bicyclo[3.1.0]hexane derivatives, selectively prepared by intramolecular cyclopropanation of sugar-derived unsaturated diazo compounds, are common precursors for the sugar moiety of cyclopentane, cyclopropane and bicyclo[3.1.0]hexane nucleosides, such as aristeromycin, the carbocyclic analogue of neplanocin C and the nucleoside A-5021.

Bicyclo[3.1.0]hexanes from sugar-derived diazo compounds and iodonium ylides. Diastereocontrol and synthetic applications

Gallos, John K,Koftis, Theocharis V,Massen, Zoe S,Dellios, Constantinos C,Mourtzinos, Ioannis T,Coutouli-Argyropoulou, Evdoxia,Koumbis, Alexandros E

, p. 8043 - 8053 (2007/10/03)

The CuI and Rh2(OAc)4 catalyzed decomposition of ethyl 2-diazo-4,5-isopropylidenedioxy-3-oxo-6-heptenoate results in intramolecular cyclopropanation products with opposite diastereoselectivity. In contrast, decomposition of the respective iodonium ylide can proceed without catalysts to give the cyclopropanation products with diastereoselectivity unchangeable by the presence of CuI and Rh2(OAc)4, revealing thus, that in this particular case the reaction is an electrophilic addition of the iodonium center to the double bond. The synthetic importance of these reactions has been demonstrated by preparing a number of precursors of cyclopentyl, cyclopropyl and bicyclo[3.1.0]hexyl antiviral carbocyclic nucleosides.

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