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6-[(4-chlorobenzyl)amino]-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 353256-69-6 Structure
  • Basic information

    1. Product Name: 6-[(4-chlorobenzyl)amino]-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione
    2. Synonyms: 6-[(4-chlorobenzyl)amino]-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione
    3. CAS NO:353256-69-6
    4. Molecular Formula: C13H14ClN3O2
    5. Molecular Weight: 279.72216
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 353256-69-6.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: 6-[(4-chlorobenzyl)amino]-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-[(4-chlorobenzyl)amino]-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione(353256-69-6)
    11. EPA Substance Registry System: 6-[(4-chlorobenzyl)amino]-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione(353256-69-6)
  • 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: 353256-69-6(Hazardous Substances Data)

353256-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 353256-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,2,5 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 353256-69:
(8*3)+(7*5)+(6*3)+(5*2)+(4*5)+(3*6)+(2*6)+(1*9)=146
146 % 10 = 6
So 353256-69-6 is a valid CAS Registry Number.

353256-69-6Downstream Products

353256-69-6Relevant articles and documents

Selective N-Monoalkylation of 6-Aminouracils with Alcohols: An Environmentally Benign Protocol for the Synthesis of 6-Alkylaminouracils

Putra, Anggi Eka,Oe, Yohei,Ohta, Tetsuo

, p. 392 - 397 (2018)

A highly selective N-alkylation of 6-aminouracils with alcohols was achieved through the borrowing hydrogen approach using iridium catalysis. 6-Aminouracils and alcohols reacted in the presence of [Cp*IrI2]2 to give 6-monoalkyluracils selectively and in high yield (up to 99 %), usually in short reaction times (2 h). These results provide a new, green, and efficient protocol for the synthesis of 6-alkylaminouracils, which are very important intermediates for the synthesis of biologically active molecules.

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