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2-(dimethylamino)-4-{4-nitrophenyl}-1,3-thiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130306-61-5 Structure
  • Basic information

    1. Product Name: 2-(dimethylamino)-4-{4-nitrophenyl}-1,3-thiazole
    2. Synonyms: 2-(dimethylamino)-4-{4-nitrophenyl}-1,3-thiazole
    3. CAS NO:130306-61-5
    4. Molecular Formula: C11H11N3O2S
    5. Molecular Weight: 249.28894
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130306-61-5.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-(dimethylamino)-4-{4-nitrophenyl}-1,3-thiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(dimethylamino)-4-{4-nitrophenyl}-1,3-thiazole(130306-61-5)
    11. EPA Substance Registry System: 2-(dimethylamino)-4-{4-nitrophenyl}-1,3-thiazole(130306-61-5)
  • 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: 130306-61-5(Hazardous Substances Data)

130306-61-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130306-61-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,3,0 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 130306-61:
(8*1)+(7*3)+(6*0)+(5*3)+(4*0)+(3*6)+(2*6)+(1*1)=75
75 % 10 = 5
So 130306-61-5 is a valid CAS Registry Number.

130306-61-5Downstream Products

130306-61-5Relevant articles and documents

Antiherpes virus compounds and methods for their preparation and use

-

, (2008/06/13)

This invention relates to methods for inhibiting herpes replication and for treating herpes infection in a mammal by inhibiting the herpes helicase-primase enzyme complex. This invention also relates to thiazolyphenyl derivatives that inhibit the herpes helicase-primase and to pharmaceutical compositions comprising the thiazolylphenyl derivatives, to methods of using and methods of producing the thiazolylphenyl derivatives

Anti-herpesvirus compounds and methods for identifying, making and using same

-

, (2008/06/13)

This invention relates to methods for inhibiting herpes replication and for treating herpes infection in a mammal by inhibiting the herpes helicase-primase enzyme complex. This invention also relates to thiazolyphenyl derivatives that inhibit the herpes helicase-primase and to pharmaceutical compositions comprising the thiazolylphenyl derivatives, to methods of using and methods of producing the thiazolylphenyl derivatives.

Electrophilic Substitution at C(5) of 2-Dimethylaminothiazoles

Mahon, Catherine M.,Meakins, G.D.

, p. 2083 - 2090 (2007/10/02)

The reactivity of a series of 4-substituted 2-dimethylaminothiazoles towards electrophiles has been examined.Acetic anhydride reacts only slowly with these thiazoles, with trichloroacetyl chloride and trifluoroacetic anhydride substitution at C(5) occurs readily.The rate of trichloroacetylation is influenced, but not to a marked extent, by changing the 4-substituent.In the presence of acid the thiazoles are deuteriated at C(5), and this reaction is much more sensitive to the nature of the 4 substituents.Estimated p Ka values of the thiazoles were used in evaluating rate constants which although only approximate, provide quantitative information about the effect of particular substituents.

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