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CAS

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1451992-80-5

(2R,3S,4R)-2,5-dithioacetyl-1,3,4-tris-p-methoxybenzyloxypentane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1451992-80-5 Structure

  • Basic information

    1. Product Name: (2R,3S,4R)-2,5-dithioacetyl-1,3,4-tris-p-methoxybenzyloxypentane
    2. Synonyms:
    3. CAS NO:1451992-80-5
    4. Molecular Formula:
    5. Molecular Weight: 628.808
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1451992-80-5.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: (2R,3S,4R)-2,5-dithioacetyl-1,3,4-tris-p-methoxybenzyloxypentane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3S,4R)-2,5-dithioacetyl-1,3,4-tris-p-methoxybenzyloxypentane(1451992-80-5)
    11. EPA Substance Registry System: (2R,3S,4R)-2,5-dithioacetyl-1,3,4-tris-p-methoxybenzyloxypentane(1451992-80-5)

  • 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: 1451992-80-5(Hazardous Substances Data)

1451992-80-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1451992-80-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,1,9,9 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1451992-80:
(9*1)+(8*4)+(7*5)+(6*1)+(5*9)+(4*9)+(3*2)+(2*8)+(1*0)=185
185 % 10 = 5
So 1451992-80-5 is a valid CAS Registry Number.

1451992-80-5Relevant articles and documents

Synthesis of a novel 1,2-dithianenucleoside via Pummerer-like reaction, followed by Vorbruggen glycosylation between a 1,2-dithiane derivative and uracil

Miyazawa, Tadashi,Umezaki, Kouhei,Tarashima, Noriko,Furukawa, Kazuhiro,Ooi, Takashi,Minakawa, Noriaki

, p. 7851 - 7853 (2013)

The novel 1,2-dithianenucleoside was designed as a hybrid type of modification between 4′-thioribonucleoside and altritol nucleoside. The desired compound, i.e., 1-[(3R,4R,5S,6R)-4,5-dihydroxy-6-hydroxymethyl-1,2- dithianyl]uracil (20), was prepared via the Pummerer-like reaction, followed by Vorbruggen glycosylation between an appropriately protected 1,2-dithiane derivative and silylated uracil.

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