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141947-30-0

2',3'-anhydro-5'-O-(4-tolylsulfonyl)-2',3'-secouridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141947-30-0 Structure

  • Basic information

    1. Product Name: 2',3'-anhydro-5'-O-(4-tolylsulfonyl)-2',3'-secouridine
    2. Synonyms:
    3. CAS NO:141947-30-0
    4. Molecular Formula:
    5. Molecular Weight: 382.394
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141947-30-0.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: 2',3'-anhydro-5'-O-(4-tolylsulfonyl)-2',3'-secouridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2',3'-anhydro-5'-O-(4-tolylsulfonyl)-2',3'-secouridine(141947-30-0)
    11. EPA Substance Registry System: 2',3'-anhydro-5'-O-(4-tolylsulfonyl)-2',3'-secouridine(141947-30-0)

  • 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: 141947-30-0(Hazardous Substances Data)

141947-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141947-30-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,9,4 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141947-30:
(8*1)+(7*4)+(6*1)+(5*9)+(4*4)+(3*7)+(2*3)+(1*0)=130
130 % 10 = 0
So 141947-30-0 is a valid CAS Registry Number.

141947-30-0Downstream Products

141947-30-0Relevant articles and documents

Regioselective Transformations of 2',3'-Seconucleosides into Anhydro Structures and Chiral Crown Ethers

Skaric, Vinko,Caplar, Vesna,Skaric, Durdica,Zinic, Mladen

, p. 493 - 506 (2007/10/02)

Intramolecular cyclisation of properly protected and activated derivatives of 2',3'-secouridine (= 1--ethyl>uracil; 1) provided access to the 2,2'-, 2,3'-, 2,5'-, 2',5'-, 3',5'-, and 2',3-anhydro-2',3'-secouridines 5, 16, 17, 26, 28 and 31, respectively (Schemes 1-3).Reaction of 2',5'-anhydro-3'-O-(methylsulfonyl)- (25) and 2',3'-anhydro-5'-O-(methylsulfonyl)-2',3'-secouridine (32) with CH2Cl2 in the presence of 1,8-diazabicycloundec-7-ene generated the N(3)-methylene-bridged bis-uridine structure 37 and 36, respectively (Scheme 3).Novel chiral 18-crown-6 ethers 40 and 44, containing a hydroxymethyl and a uracil-1-yl or adenin-9-yl as the pendant groups in a 1,3-cis relationship, were synthesized from 5'-O-(triphenylmethyl)-2',3'-secouridine (2) and 5'-O,N6-bis(triphenylmethyl)-2',3'-secoadenosine (41) on reaction with 3,6,9-trioxaundecane-1,11-diyl bis(4-toluenesulfonate) and detritylation of the thus obtained (triphenylmethoxy)methyl compound 39 and 43, respectively (Scheme 4).

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