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950664-85-4

1,3-dibenzyl-5-nitro-6-phenethylpyrimidine-2,4(1H,3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 950664-85-4 Structure

  • Basic information

    1. Product Name: 1,3-dibenzyl-5-nitro-6-phenethylpyrimidine-2,4(1H,3H)-dione
    2. Synonyms: 1,3-dibenzyl-5-nitro-6-phenethylpyrimidine-2,4(1H,3H)-dione
    3. CAS NO:950664-85-4
    4. Molecular Formula:
    5. Molecular Weight: 441.486
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 950664-85-4.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: 1,3-dibenzyl-5-nitro-6-phenethylpyrimidine-2,4(1H,3H)-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-dibenzyl-5-nitro-6-phenethylpyrimidine-2,4(1H,3H)-dione(950664-85-4)
    11. EPA Substance Registry System: 1,3-dibenzyl-5-nitro-6-phenethylpyrimidine-2,4(1H,3H)-dione(950664-85-4)

  • 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: 950664-85-4(Hazardous Substances Data)

950664-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 950664-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,0,6,6 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 950664-85:
(8*9)+(7*5)+(6*0)+(5*6)+(4*6)+(3*4)+(2*8)+(1*5)=194
194 % 10 = 4
So 950664-85-4 is a valid CAS Registry Number.

950664-85-4Relevant articles and documents

Synthesis of 1-(alkyl)-5-dimethylamino-6-phenethyluracils as potent nonnucleoside HIV-1 RT inhibitors

Wang, Xiaowei,Chen, Yanli,Guo, Ying,Li, Amin,Ma, Xiaoyan,Liu, Junyi

, p. 2421 - 2431 (2008/02/10)

1-(Alkyl)-5-dimethylamino-6-phenethyl uracils (1) and (2) are analogs of MKC-442, which is a very potent inhibitor of HIV-1 reverse transcriptase. The target compound 1 was synthesized by the first approach, from the corresponding 1,3-dibenzyl-5-(dimethylamino)-6-phenethylpyrimidine-2,4(1H,3H)-dione (7), which was synthesized in four steps from 6-methyluracil (3) by nitration, benzylation, reduction, and methylation of the amino group. Compound 7 was then debenzylated to give the complete deprotected compound 8 with very low yield. To improve the yield, another pathway was developed for introducing the ethoxymethyl group at N-1 of the uracil ring first. The result of adjusting reaction sequences increased the overall yield dramatically. All synthesized compounds were tested for their inhibition of HIV-1 reverse transcriptase, and moderate activity was found for target compound 1. Copyright Taylor & Francis Group, LLC.

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