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151359-62-5

Oxazole, 4,5-bis(4-chlorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 151359-62-5 Structure

  • Basic information

    1. Product Name: Oxazole, 4,5-bis(4-chlorophenyl)-
    2. Synonyms:
    3. CAS NO:151359-62-5
    4. Molecular Formula: C15H9Cl2NO
    5. Molecular Weight: 290.149
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 151359-62-5.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: Oxazole, 4,5-bis(4-chlorophenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Oxazole, 4,5-bis(4-chlorophenyl)-(151359-62-5)
    11. EPA Substance Registry System: Oxazole, 4,5-bis(4-chlorophenyl)-(151359-62-5)

  • 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: 151359-62-5(Hazardous Substances Data)

151359-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151359-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,3,5 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 151359-62:
(8*1)+(7*5)+(6*1)+(5*3)+(4*5)+(3*9)+(2*6)+(1*2)=125
125 % 10 = 5
So 151359-62-5 is a valid CAS Registry Number.

151359-62-5Relevant articles and documents

Synthesis, biological evaluation, and molecular modeling studies of novel heterocyclic compounds as anti-proliferative agents

Chaudhary, Anurag,Sharma,Bhardwaj, Gautam,Jain, Vaibhav,Bharatam,Shrivastav, Birendra,Roy

, p. 5654 - 5669 (2013)

Two novel series of heterocyclic compounds have been synthesized. In first series, isatin was allowed to react with substituted aromatic/cyclic carbonyl compounds to get desired mannich bases (2a-e). In second series, 4,5-disubstituted oxazoles (6a-p) wer

Synthesis and activity of 4,5-diarylimidazoles as human CB1 receptor inverse agonists

Plummer, Christopher W.,Finke, Paul E.,Mills, Sander G.,Wang, Junying,Tong, Xinchun,Doss, George A.,Fong, Tung M.,Lao, Julie Z.,Schaeffer, Marie-Therese,Chen, Jing,Shen, Chun-Pyn,Stribling, D. Sloan,Shearman, Lauren P.,Strack, Alison M.,Van Der Ploeg, Lex H.T.

, p. 1441 - 1446 (2007/10/03)

Structure-activity relationship studies directed toward the optimization of 4,5-diarylimidazole-2-carboxamide analogs as human CB1 receptor inverse agonists resulted in the discovery of the two amide derivatives 24a and b (hCB1 IC50 = 6.1 and 4

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