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1400767-11-4

C30H22Br2N2OS is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1400767-11-4 Structure

  • Basic information

    1. Product Name: C30H22Br2N2OS
    2. Synonyms: C30H22Br2N2OS
    3. CAS NO:1400767-11-4
    4. Molecular Formula:
    5. Molecular Weight: 618.391
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1400767-11-4.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: C30H22Br2N2OS(CAS DataBase Reference)
    10. NIST Chemistry Reference: C30H22Br2N2OS(1400767-11-4)
    11. EPA Substance Registry System: C30H22Br2N2OS(1400767-11-4)

  • 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: 1400767-11-4(Hazardous Substances Data)

1400767-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1400767-11-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,0,7,6 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1400767-11:
(9*1)+(8*4)+(7*0)+(6*0)+(5*7)+(4*6)+(3*7)+(2*1)+(1*1)=124
124 % 10 = 4
So 1400767-11-4 is a valid CAS Registry Number.

1400767-11-4Downstream Products

1400767-11-4Relevant articles and documents

One pot efficient diversity oriented synthesis of polyfunctional styryl thiazolopyrimidines and their bio-evaluation as antimalarial and anti-HIV agents

Fatima, Seerat,Sharma, Anindra,Saxena, Reshu,Tripathi, Rajkamal,Shukla, Sanjeev K.,Pandey, Swaroop Kumar,Tripathi, Renu,Tripathi, Rama P.

, p. 195 - 204 (2012)

An efficient one pot synthesis of a series of pluripotent (E)-1-(3-methyl-5-aryl-7-styryl-5H-thiazolo[3,2-a]pyrimidin-6-yl) -3-arylprop-2-en-1-ones is reported. It involves reaction of 5-acetyl-6-methyl-4-aryl-dihydropyrimidine-2-thiones, propargyl bromide and aromatic aldehydes in presence of ethanolic KOH. The newly synthesized compounds were evaluated for antimalarial activity against Plasmodium falciparum and as HIV-RT inhibitors. Most of the compound displayed potent antimalarial activity with IC50 2 μg/mL. Compounds 6, 11 and 20 showed better activity against P. falciparum K1 strains in comparison to standard drug chloroquine. Compounds 6, 11, and 16 exhibited 73.44, 66.92, and 70.81% HIV-RT inhibition at 100 μg/mL.

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