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76979-35-6

2-methylthio-5-p-chlorophenylmethylene-thiazolinone-4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76979-35-6 Structure

  • Basic information

    1. Product Name: 2-methylthio-5-p-chlorophenylmethylene-thiazolinone-4
    2. Synonyms: 2-methylthio-5-p-chlorophenylmethylene-thiazolinone-4
    3. CAS NO:76979-35-6
    4. Molecular Formula:
    5. Molecular Weight: 269.776
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76979-35-6.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: 2-methylthio-5-p-chlorophenylmethylene-thiazolinone-4(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methylthio-5-p-chlorophenylmethylene-thiazolinone-4(76979-35-6)
    11. EPA Substance Registry System: 2-methylthio-5-p-chlorophenylmethylene-thiazolinone-4(76979-35-6)

  • 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: 76979-35-6(Hazardous Substances Data)

76979-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76979-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,7 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76979-35:
(7*7)+(6*6)+(5*9)+(4*7)+(3*9)+(2*3)+(1*5)=196
196 % 10 = 6
So 76979-35-6 is a valid CAS Registry Number.

76979-35-6Relevant articles and documents

Synthesis and antimicrobial activity of 5-substitued 4-thiazolidinones with sulfanilamide pharmacophore

Zevzikoviene, Augusta,Zevzikovas, Andrejus,Lukosius, Audronis,Tarasevicius, Eduardas

, p. 1155 - 1161 (2016/10/17)

After incorporation pharmacophores of allylamine and sulfanilamide into 4-thiazolidinone's ring - no antimicrobial activity was determined. This outcome stimulated synthesis of new group - 5-substituted 4-thiazolidinones. In the literature it is noted tha

Combination of 4-anilinoquinazoline and rhodanine as novel epidermal growth factor receptor tyrosine kinase inhibitors

Li, Si-Ning,Xu, Yun-Yun,Gao, Jia-Yu,Yin, Hong-Ran,Zhang, Shi-Lei,Li, Huan-Qiu

, p. 3221 - 3227 (2015/08/03)

Abstract A type of novel rhodanine-based 4-anilinoquinazoline, which designed the combination between quinazoline as the backbone and various substituted biological rhodanine groups as the side chain, have been synthesized, and their antiproliferative act

INTRODUCTION OF SELENIUM TO HETEROCYCLIC COMPOUNDS. PART II. SYNTHESIS OF 3-ALKYL-2-SELENOHYDANTOINS, 2-SELENOHYDANTOIN-3-ACETIC ACID AND 2-SELENORHODANINES WITH DOUBLE BOND AT C-5

Korohoda, Maria Jolanta

, p. 359 - 369 (2007/10/02)

The earlier described method was applied to synthesize so far unknown benzylidene derivatives of 3-methyl-2-selenohydantoin, 2-selenohydantoin-3-acetic acid and 2-selenorhodanine.The structures of these compounds were confirmed by the spectral data.Some p

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