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147526-02-1

(+/-)-4-(2-phenylethyl)-2-azetidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 147526-02-1 Structure

  • Basic information

    1. Product Name: (+/-)-4-(2-phenylethyl)-2-azetidinone
    2. Synonyms: (+/-)-4-(2-phenylethyl)-2-azetidinone
    3. CAS NO:147526-02-1
    4. Molecular Formula:
    5. Molecular Weight: 175.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 147526-02-1.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-(2-phenylethyl)-2-azetidinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-4-(2-phenylethyl)-2-azetidinone(147526-02-1)
    11. EPA Substance Registry System: (+/-)-4-(2-phenylethyl)-2-azetidinone(147526-02-1)

  • 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: 147526-02-1(Hazardous Substances Data)

147526-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147526-02-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,5,2 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 147526-02:
(8*1)+(7*4)+(6*7)+(5*5)+(4*2)+(3*6)+(2*0)+(1*2)=131
131 % 10 = 1
So 147526-02-1 is a valid CAS Registry Number.

147526-02-1Relevant articles and documents

Total synthesis and immunosuppressive activity of (-)-pateamine A and related compounds: Implementation of a β-lactam-based macrocyclization

Romo, Daniel,Rzasa, Robert M.,Shea, Helene A.,Park, Kaapjoo,Langenhan, Joseph M.,Sun, Luo,Akhiezer, Alexander,Liu, Jun O.

, p. 12237 - 12254 (2007/10/03)

The asymmetric synthesis of the potent immunosuppressive agent (-)- pateamine A isolated from the marine sponge Mycale sp. is described. A key strategy employed in the synthesis was a β-lactam-based macrocyclization to form the 19-membered dilactone macrolide. The synthesis confirms the relative and absolute stereochemistry as 3R,5S, 10S,24S and sets the stage for studies into the mechanism of action of pateamine A. Other studies and findings made in the course of the synthesis and described herein include the following: (1) a Stille coupling can be competitive with π-allyl formation, (2) SmI2 effects a mild N-O cleavage of N-benzyloxy-β-lactams, (3) the synthesis of a pateamine A-dexamethasone hybrid molecule for use in a yeast three-hybrid assay was accomplished, and (4) IC50 values were determined for synthetic and natural pateamine A and related compounds in the interleukin 2 reporter gene assay.

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