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706769-70-2

C14H11BrN4O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 706769-70-2 Structure

  • Basic information

    1. Product Name: C14H11BrN4O3S
    2. Synonyms:
    3. CAS NO:706769-70-2
    4. Molecular Formula:
    5. Molecular Weight: 395.236
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 706769-70-2.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: C14H11BrN4O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H11BrN4O3S(706769-70-2)
    11. EPA Substance Registry System: C14H11BrN4O3S(706769-70-2)

  • 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: 706769-70-2(Hazardous Substances Data)

706769-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 706769-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,6,7,6 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 706769-70:
(8*7)+(7*0)+(6*6)+(5*7)+(4*6)+(3*9)+(2*7)+(1*0)=192
192 % 10 = 2
So 706769-70-2 is a valid CAS Registry Number.

706769-70-2Relevant articles and documents

Synthesis of new 1,2,4-Triazole-5-thiones and their thioglycoside derivatives as potential antibacterial agents

Dilmaghani, Karim Akbari,Nasuhi Pur, Fazel,Jazani, Nima Hoseini,Alavi, Asma,Niknam, Zahra,Mirfakhraee, Farrin

, p. 81 - 87 (2014)

Abstract The glycosylation of 1,2,4-triazole-5-thiones has been performed with peracetylated β-pyranosyl bromide in the presence of potassium carbonate. The synthesized compounds were tested for their antimicrobial activity against bacterial (Gram-negative and Gram-positive) and yeasts strains in vitro. The synthetic compounds showed different inhibition zones against tested bacterial and yeasts strains. Among them, compounds which possessed 2-furyl and p-bromophenyl moieties showed the best results against Acinetobacter calcoaceticus ATCC 23055.

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