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142764-13-4

1,2,5-Oxadiazole, 3-[(4-fluorophenyl)thio]-4-methyl-, 2-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 142764-13-4 Structure

  • Basic information

    1. Product Name: 1,2,5-Oxadiazole, 3-[(4-fluorophenyl)thio]-4-methyl-, 2-oxide
    2. Synonyms:
    3. CAS NO:142764-13-4
    4. Molecular Formula: C9H7FN2O2S
    5. Molecular Weight: 226.231
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 142764-13-4.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: 1,2,5-Oxadiazole, 3-[(4-fluorophenyl)thio]-4-methyl-, 2-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2,5-Oxadiazole, 3-[(4-fluorophenyl)thio]-4-methyl-, 2-oxide(142764-13-4)
    11. EPA Substance Registry System: 1,2,5-Oxadiazole, 3-[(4-fluorophenyl)thio]-4-methyl-, 2-oxide(142764-13-4)

  • 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: 142764-13-4(Hazardous Substances Data)

142764-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142764-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,6 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 142764-13:
(8*1)+(7*4)+(6*2)+(5*7)+(4*6)+(3*4)+(2*1)+(1*3)=124
124 % 10 = 4
So 142764-13-4 is a valid CAS Registry Number.

142764-13-4Relevant articles and documents

Pharmacochemistry of the furoxan ring: Recent developments

Calvino,Di Stilo,Fruttero,Gasco,Sorba,Gasco

, p. 321 - 334 (2007/10/02)

In the present work recent results obtained in the pharmacochemistry of the furoxan system are reported. In particular, after a brief description of the salient points of the furoxan chemistry, the synthesis and the properties of a series of Nifedipine and Prazosin analogues, containing this heterocyclic system, are described. Since we observed that a few furoxan derivatives are able to elicit both a dose-dependent rise in platelet cGMP levels and to promote a dose-dependent inhibition of AA-induced [Ca++] rise, and that many substituted furoxans show potent vasodilating and antiaggregatory activity, the possibility of using the furoxan system as a lead in the design of new vasodilators is also discussed.

4-Methyl-3-(arylsulfonyl)furoxans: A New Class of Potent Inhibitors of Platelet Aggregation

Calvino, R.,Fruttero, R.,Ghigo, D.,Bosia, A.,Pescarmona, G. P.,Gasco, A.

, p. 3296 - 3300 (2007/10/02)

A series of 4-methyl-3-(arylthio)furoxans were synthesized by oxidation of 1-(arylthio)-2-methylglyoxymes with dinitrogen tetroxide.Reduction with trimethyl phosphite of the furoxan derivatives afforded the corresponding furazans, while oxidation with an

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