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4-(5-methyl-4-phenylthiazol-2-yl)benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1292686-21-5 Structure
  • Basic information

    1. Product Name: 4-(5-methyl-4-phenylthiazol-2-yl)benzoic acid
    2. Synonyms: 4-(5-methyl-4-phenylthiazol-2-yl)benzoic acid
    3. CAS NO:1292686-21-5
    4. Molecular Formula:
    5. Molecular Weight: 295.362
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1292686-21-5.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-(5-methyl-4-phenylthiazol-2-yl)benzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(5-methyl-4-phenylthiazol-2-yl)benzoic acid(1292686-21-5)
    11. EPA Substance Registry System: 4-(5-methyl-4-phenylthiazol-2-yl)benzoic acid(1292686-21-5)
  • 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: 1292686-21-5(Hazardous Substances Data)

1292686-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1292686-21-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,2,6,8 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1292686-21:
(9*1)+(8*2)+(7*9)+(6*2)+(5*6)+(4*8)+(3*6)+(2*2)+(1*1)=185
185 % 10 = 5
So 1292686-21-5 is a valid CAS Registry Number.

1292686-21-5Downstream Products

1292686-21-5Relevant articles and documents

Synthesis and applications of 2,4-disubstituted thiazole derivatives as small molecule modulators of cellular development

Zhou, Garr-Layy,Tams, Daniel M.,Marder, Todd B.,Valentine, Roy,Whiting, Andrew,Przyborski, Stefan A.

, p. 2323 - 2334 (2013/04/10)

Understanding how the structure of molecules relates to their function and biological activity is essential in the development of new analogues with targeted activity. This is especially relevant in mediating developmental processes in mammalian cells and the regulation of stem cell differentiation. In this study, thiazole-containing small molecules were synthesised and investigated for their ability to induce the differentiation of human pluripotent stem cells and their derivatives. Analyses of cell morphology, cell viability, expression of cell surface markers and ability to induce cell differentiation and regulate neurite formation identified the analogue with the longest and most bulky hydrophobic side chain as possessing comparable or enhanced activity to all-trans-retinoic acid (ATRA). Interestingly, a shorter, less bulky, known thiazole compound reported to be isoform selective for the retinoic acid receptor β2 (RARβ2) agonist did not mediate differentiation under the conditions tested; however, activity could be restored by adjusting the structure to a longer, more bulky molecule. These data provide further insight into the complexity of compound design in terms of developing small molecules with specific biological activities to control the development and differentiation of mammalian cells.

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