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132981-94-3

4-phenyl-5-(p-tolyl)thiazol-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132981-94-3 Structure

  • Basic information

    1. Product Name: 4-phenyl-5-(p-tolyl)thiazol-2-amine
    2. Synonyms: 4-phenyl-5-(p-tolyl)thiazol-2-amine
    3. CAS NO:132981-94-3
    4. Molecular Formula:
    5. Molecular Weight: 266.367
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132981-94-3.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: 4-phenyl-5-(p-tolyl)thiazol-2-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-phenyl-5-(p-tolyl)thiazol-2-amine(132981-94-3)
    11. EPA Substance Registry System: 4-phenyl-5-(p-tolyl)thiazol-2-amine(132981-94-3)

  • 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: 132981-94-3(Hazardous Substances Data)

132981-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132981-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,8 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132981-94:
(8*1)+(7*3)+(6*2)+(5*9)+(4*8)+(3*1)+(2*9)+(1*4)=143
143 % 10 = 3
So 132981-94-3 is a valid CAS Registry Number.

132981-94-3Downstream Products

132981-94-3Relevant articles and documents

SUBSTITUTED PROPANAMIDES AS INHIBITORS OF NUCLEASES

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Page/Page column 11; 13; 23; 24; 26, (2019/11/12)

The invention provides compounds represented by the structural formula (1): wherein R1, R2, R3, R4, R5, R6 are as defined in the claims. The compounds are inhibitors of nucleases, and are useful in particular in a method of treatment and/or prevention of proliferative diseases, neurodegenerative diseases, and other genomic instability associated diseases.

Synthesis of 5-Phenylthiazolamines by Using Thiourea as an α-Bromination Shuttle

Roslan, Irwan Iskandar,Ng, Kian-Hong,Chuah, Gaik-Khuan,Jaenicke, Stephan

, p. 704 - 709 (2017/02/05)

A straightforward synthesis of 5-phenylthiazolamines by coupling thiourea with phenylacetones, phenylacetophenones, and β-tetralone has been developed. Thiourea acts as a substrate and an α-bromination shuttle by transferring a Br atom from CBrCl3/s

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