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155782-81-3

Z-4-methylstyrylthioacetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 155782-81-3 Structure

  • Basic information

    1. Product Name: Z-4-methylstyrylthioacetic acid
    2. Synonyms: Z-4-methylstyrylthioacetic acid
    3. CAS NO:155782-81-3
    4. Molecular Formula:
    5. Molecular Weight: 208.281
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 155782-81-3.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: Z-4-methylstyrylthioacetic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: Z-4-methylstyrylthioacetic acid(155782-81-3)
    11. EPA Substance Registry System: Z-4-methylstyrylthioacetic acid(155782-81-3)

  • 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: 155782-81-3(Hazardous Substances Data)

155782-81-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155782-81-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,7,8 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 155782-81:
(8*1)+(7*5)+(6*5)+(5*7)+(4*8)+(3*2)+(2*8)+(1*1)=163
163 % 10 = 3
So 155782-81-3 is a valid CAS Registry Number.

155782-81-3Relevant articles and documents

Synthesis and antimicrobial activity of styryl/pyrrolyl/pyrazolyl sulfonylmethyl-1,3,4-oxadiazolyl amines and styryl/pyrrolyl/pyrazolyl sulfonylmethyl-1,3,4-thiadiazolyl amines

Sravya,Yamini,Padmavathi,Padmaja

, p. 647 - 655 (2016)

A new class of mono and bis heterocycles - styryl sulfonylmethyl-1,3,4-oxadiazolyl/1,3,4-thiadiazolyl amines, pyrrolyl sulfonylmethyl-1,3,4-oxadiazolyl/1,3,4-thiadiazolyl amines and pyrazolyl sulfonylmethyl-1,3,4-oxadiazolyl/1,3,4-thiadiazolyl amines were

Synthesis, antioxidant and anti-inflammatory activities of 5-((styrylsulfonyl) methyl)-1,3,4-oxadiazol / thiadiazol-2-amine derivatives

Nagarjuna, Ummadi,Padmaja, Adivireddy,Padmavathi, Venkatapuram,Priya, Sakuri Chandi,Rajitha, Galla,Sravya, Gundala

, p. 1233 - 1247 (2019/11/22)

Background: A new class of 5-(styrylsulfonylmethyl)-1,3,4-oxadiazol-2-amine and 5- (styrylsulfonylmethyl)-1,3,4-thiadiazol-2-amine derivatives were prepared by derivatization of amino function. Methods: All the synthesized compounds were tested for antiox

Tetrahydro-1,4-thiazine-1,1-dioxides: Part IV - Synthesis and conformational analysis of some 2,3,5-trisubstituted tetrahydro-1,4-thiazine-1,1-dioxides

Reddy, D. Bhaskar,Reddy, M. Muralidhar,Subbaraju, Gottumukkala V.

, p. 816 - 822 (2007/10/03)

A series of new 2-aroyl-3,5-diaryltetrahydro-1,4-thiazine-1,1-dioxides (2) has been synthesized either from phenacylsulfonylacetic acids (1) or phenacylstyrylsulfones (3), which in turn are obtained from the substituted acetophenones or styrenes, respecti

A NEW APPROACH TO THE SYNTHESIS OF ISOMERIC E,Z- AND E,E-BIS(STYRYL)SULFONES AND A STUDY OF THEIR CYCLOPROPANATION

Reddy, D. Bhaskar,Reddy, P. V. Ramana,Vijayalakshmi, S.,Reddy, M. V. Ramana

, p. 63 - 72 (2007/10/02)

The E,Z- and E,E-bis(styryl)sulfones (V and X) have benn synthesized from 4-methylphenylacetylene (1) and 4-methylstyrene (VI), respectively.The cyclopropanation of V and X with dimethylsulfoxonium methylide by PTC or Corey and Chaykovsky methods gave E,E

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