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1170086-89-1

4-oxo-4H-chromene-3-carbothioic acid N-phenylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1170086-89-1 Structure

  • Basic information

    1. Product Name: 4-oxo-4H-chromene-3-carbothioic acid N-phenylamide
    2. Synonyms: 4-oxo-4H-chromene-3-carbothioic acid N-phenylamide
    3. CAS NO:1170086-89-1
    4. Molecular Formula:
    5. Molecular Weight: 281.335
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1170086-89-1.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: 4-oxo-4H-chromene-3-carbothioic acid N-phenylamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-oxo-4H-chromene-3-carbothioic acid N-phenylamide(1170086-89-1)
    11. EPA Substance Registry System: 4-oxo-4H-chromene-3-carbothioic acid N-phenylamide(1170086-89-1)

  • 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: 1170086-89-1(Hazardous Substances Data)

1170086-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1170086-89-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,0,0,8 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1170086-89:
(9*1)+(8*1)+(7*7)+(6*0)+(5*0)+(4*8)+(3*6)+(2*8)+(1*9)=141
141 % 10 = 1
So 1170086-89-1 is a valid CAS Registry Number.

1170086-89-1Relevant articles and documents

Synthesis of 2-aminochromone-3-carbaldehyde hydrazones from 3-thiocarbamoylchromones and hydrazines

Demin, D. Yu.,Rodionova,Yarovenko,Krayushkin

, p. 2054 - 2057 (2018)

Reaction of 3-thiocarbamoylchromones with hydrazines is accompanied by recyclization affording 2-aminochromone-3-carbaldehyde hydrazones.

Unusual transformations of 3-thiocarbamoylchromones

Demin, Dmitrii Y.,Fakhrutdinov, Artem N.,Ilyasov, Igor R.,Baryshnikova, Tatyana K.,Krayushkin, Mikhail M.,Yarovenko, Vladimir N.

, (2020)

The reaction of malononitrile with 3-thiocarbamoylchromones was accompanied by rearrangement, resulting in the formation of 2,5-dihydro-1H-chromeno[2,3-b]pyridine-3-carbonitriles or 2-imino-5-oxo-1-phenyl-2,5-dihydro-1H-chromeno[2,3-b]pyridine-3-carbothio

Cytotoxic activity of 3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones and 4-oxo-4H-chromene-3-carbothioic acid N-phenylamides

Raj, Tilak,Bhatia, Richa Kaur,kapur, Ashish,Sharma, Madhunika,Saxena,Ishar

scheme or table, p. 790 - 794 (2010/04/04)

6/6,7-Substituted-3-formylchromones (8a-g) were reacted with 2 equivalents thiobenzamide (9) in refluxing toluene to furnish substituted-3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones (10a-g) in high yields. Similarly, when substituted-2-anilino-3-formylchromones (8a-d) were reacted with thiobenzamide (9, 2 equivalents) in refluxing xylene, 4-oxo-4H-chromene-3-carbothioic acid N-phenylamides (11a-d) were obtained in high yields. All the compounds (10a-g) and (11a-d) display significant cytotoxic activity against a number of human cancer cell lines. Among these compounds 10e (IC50?=?10?μM), 10b (IC50?=?14.6?μM) and 10a (IC50?=?10.5?μM) showed maximum cytotoxic activity on neuroblastoma. Also, the compound 10c (IC50?=?10.5?μM) showed maximum cytotoxic activity on ovarian cancer cell line.

Mechanism of unusual formation of 3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones and 4-oxo-4H-chromene-3-carbothioic acid N-phenylamides and their antimicrobial evaluation

Raj, Tilak,Bhatia, Richa Kaur,Sharma, Rakesh Kumar,Gupta, Vivek,Sharma, Deepak,Ishar, Mohan Paul Singh

experimental part, p. 3209 - 3216 (2009/10/23)

6/6,7-Substituted 3-formylchromones (9a-e) react with 2 equivalents of 2-phenyl-4-dimethylamino-1-thia-3-azabuta-1,3-diene (10) or thiobenzamide (11) in refluxing toluene to furnish novel substituted 3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones (12

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