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CAS

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353260-19-2

2-[(3-fluorobenzyl)sulfanyl]-4(3H)-pyrimidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 353260-19-2 Structure

  • Basic information

    1. Product Name: 2-[(3-fluorobenzyl)sulfanyl]-4(3H)-pyrimidinone
    2. Synonyms: 2-[(3-fluorobenzyl)sulfanyl]-4(3H)-pyrimidinone
    3. CAS NO:353260-19-2
    4. Molecular Formula: C11H9FN2OS
    5. Molecular Weight: 236.2653632
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 353260-19-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[(3-fluorobenzyl)sulfanyl]-4(3H)-pyrimidinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[(3-fluorobenzyl)sulfanyl]-4(3H)-pyrimidinone(353260-19-2)
    11. EPA Substance Registry System: 2-[(3-fluorobenzyl)sulfanyl]-4(3H)-pyrimidinone(353260-19-2)

  • 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: 353260-19-2(Hazardous Substances Data)

353260-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 353260-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,2,6 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 353260-19:
(8*3)+(7*5)+(6*3)+(5*2)+(4*6)+(3*0)+(2*1)+(1*9)=122
122 % 10 = 2
So 353260-19-2 is a valid CAS Registry Number.

353260-19-2Relevant articles and documents

4-Aminopyrimidine libraries from the Ugi-Smiles reaction of thiouracil

Sidhoum, Madjid Ait,El Ka?m, Laurent,Grimaud, Laurence

, p. 5222 - 5231 (2018/05/04)

The Ugi-Smiles reaction of S-benzyl thiouracil have been exploited in several three-step sequences for the preparation of aminopyrimidine libraries with high diversity. After the 4-component coupling, oxidation of the thioether to sulfone is followed by displacement of the latter by various carbon-centered nucleophiles (cyanide, malonate, boronic acids) or amines. The efficiency of the whole sequence was further demonstrated with one-pot procedures.

Ugi-smiles coupling of thiouracil derivatives towards 2,4-diamino pyrimidines

Sidhoum, Madjid Ait,Ka?m, Laurent El,Grimaud, Laurence

supporting information; experimental part, p. 632 - 636 (2012/04/11)

Diaminopyrimidines could be synthesized via a multicomponent coupling starting from S-alkyl thiouracil derivatives. The synthetic strategy based upon an Ugi-Smiles coupling, and subsequent oxidation of the adducts affords a versatile platform for the prep

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