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37592-55-5

N-(2'-Chlorezhyl)-2-hydroxybenzamid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 37592-55-5 Structure

  • Basic information

    1. Product Name: N-(2'-Chlorezhyl)-2-hydroxybenzamid
    2. Synonyms:
    3. CAS NO:37592-55-5
    4. Molecular Formula:
    5. Molecular Weight: 199.637
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 37592-55-5.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: N-(2'-Chlorezhyl)-2-hydroxybenzamid(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2'-Chlorezhyl)-2-hydroxybenzamid(37592-55-5)
    11. EPA Substance Registry System: N-(2'-Chlorezhyl)-2-hydroxybenzamid(37592-55-5)

  • 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: 37592-55-5(Hazardous Substances Data)

37592-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37592-55-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,9 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 37592-55:
(7*3)+(6*7)+(5*5)+(4*9)+(3*2)+(2*5)+(1*5)=145
145 % 10 = 5
So 37592-55-5 is a valid CAS Registry Number.

37592-55-5Relevant articles and documents

Living cationic ring-opening polymerization of 2-oxazolines initiated by rare-earth metal triflates

Hu, Fangyu,Xie, Shoulei,Jiang, Liming,Shen, Zhiquan

, p. 59917 - 59926 (2014)

The cationic ring-opening polymerization (CROP) of substituted 2-oxazolines using rare-earth metal triflates (RE(OTf)3) as initiator was investigated for the first time. In this work, we examined the polymerization characteristics of 2-ethyl-2-oxazoline (EtOx) initiated by Sc(OTf)3 under conventional thermal heating and microwave irradiation, and compared the respective outcomes with those obtained with the most frequently used initiator methyl tosylate (MeOTs). The results indicated that Sc(OTf)3 exhibits a higher catalytic efficiency to the EtOx polymerization than MeOTs under identical conditions. The controlled/living nature of the Sc(OTf)3-catalyzed CROP was confirmed by its linear first-order kinetics and the narrow molecular weight distribution of the resultant polymers as well as the block copolymerization of EtOx and 2-phenyl-2-oxazoline (PhOx). Based on in situ NMR spectroscopic studies and SEC analysis of PEtOx samples obtained from the control termination experiments, a possible initiating/propagating mechanism has been proposed for the living cationic ring-opening polymerization. Morever, this rare-earth catalytic system can also be applied to the ring-opening polymerization of some sterically hindered or aryl-substituted 2-oxazolines.

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