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144410-27-5

Aids004839 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144410-27-5 Structure

  • Basic information

    1. Product Name: Aids004839
    2. Synonyms: 1-Etome-6diclphs-5et u;Aids004839;Aids-004839
    3. CAS NO:144410-27-5
    4. Molecular Formula: C15H16Cl2N2O3S
    5. Molecular Weight: 375.27014
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144410-27-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: °Cat760mmHg
    3. Flash Point: °C
    4. Appearance: /
    5. Density: 1.43g/cm3
    6. Refractive Index: 1.627
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Aids004839(CAS DataBase Reference)
    10. NIST Chemistry Reference: Aids004839(144410-27-5)
    11. EPA Substance Registry System: Aids004839(144410-27-5)

  • 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: 144410-27-5(Hazardous Substances Data)

144410-27-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144410-27-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,1 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 144410-27:
(8*1)+(7*4)+(6*4)+(5*4)+(4*1)+(3*0)+(2*2)+(1*7)=95
95 % 10 = 5
So 144410-27-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H16Cl2N2O3S/c1-3-12-13(20)18-15(21)19(8-22-4-2)14(12)23-11-6-9(16)5-10(17)7-11/h5-7H,3-4,8H2,1-2H3,(H,18,20,21)

144410-27-5Downstream Products

144410-27-5Relevant articles and documents

Synthesis and Antiviral Activity of Deoxy Analogs of 1--6-(phenylthio)thymine (HEPT) as Potent and Selective Anti-HIV-1 Agents

Tanaka, Hiromichi,Takashima, Hideaki,Ubasawa, Masaru,Sekiya, Kouichi,Nitta, Issei,et al.

, p. 4713 - 4719 (2007/10/02)

The effect of substitution in the acyclic structure of 1--6-(phenylthio)thymine (HEPT) on anti-HIV-1 activity was investigated by synthesizing a series of deoxy analogs and related compounds.Preparation of 1-(2-alkyloxyethoxy)met

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