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1391014-03-1

C19H19N5OS2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1391014-03-1 Structure

  • Basic information

    1. Product Name: C19H19N5OS2
    2. Synonyms: C19H19N5OS2
    3. CAS NO:1391014-03-1
    4. Molecular Formula:
    5. Molecular Weight: 397.525
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1391014-03-1.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: C19H19N5OS2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H19N5OS2(1391014-03-1)
    11. EPA Substance Registry System: C19H19N5OS2(1391014-03-1)

  • 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: 1391014-03-1(Hazardous Substances Data)

1391014-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1391014-03-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,1,0,1 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1391014-03:
(9*1)+(8*3)+(7*9)+(6*1)+(5*0)+(4*1)+(3*4)+(2*0)+(1*3)=121
121 % 10 = 1
So 1391014-03-1 is a valid CAS Registry Number.

1391014-03-1Relevant articles and documents

Synthesis, characterization and evaluation of antimicrobial activity of some novel 1,2,4-triazoles and 1,3,4-thiadiazoles bearing imidazole nuclues

Aouad, Mohamed Reda,Rezki, Nadjet,Kasmi, Mohamed,Aouad, Linda,Rezki, Merieme A.

experimental part, p. 1141 - 1154 (2012/09/07)

A series of N1-[(4,5-di and 1,4,5-triphenylimidazol-2-yl) thioacetyl]- N4-alkyl/aryl-thiosemicarbazides 3-7 were synthesized from (4,5-di and 3,4,5- triphenylimidazol-2-yl)thioacetic acid hydrazide 1, 2. The treatment of compounds 3-7 with NaOH gave 5-[(4,5-di and 1,4,5-triphenylimidazol-2-yl)-3- thiomethyl]-4-alkyl/aryl-2H-1,2,4-triazoles-3- thione 8-12, while the acidic treatment of compounds 3-7 afforded 5-[(4,5-di- and 1,4,5-triphenylimidazol-2- yl)-3-thiomethyl]-2-alkyl/arylamino-1,3,4- thiadiazoles 13-17. Moreover, potassium hydrazinecarbothionates 18, 19 were obtained from the reaction of acyl hydrazides 1, 2 with carbon disulfides in basic media and converted into 4-amino- 1,2,4-triazole-3-thiones 20, 21 and 1,3,4-thiadiazole-2-thiols 22, 23 by the treatment with hydrazine hydrate and sulfuric acid, respectively. All newly synthesized compounds were screened for their antimicrobial activity.

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