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291279-17-9

N-Boc-4-benzyl-5-chloromethyl-5-hydroxy-3-oxazolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 291279-17-9 Structure

  • Basic information

    1. Product Name: N-Boc-4-benzyl-5-chloromethyl-5-hydroxy-3-oxazolidine
    2. Synonyms: N-Boc-4-benzyl-5-chloromethyl-5-hydroxy-3-oxazolidine
    3. CAS NO:291279-17-9
    4. Molecular Formula:
    5. Molecular Weight: 327.808
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 291279-17-9.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-Boc-4-benzyl-5-chloromethyl-5-hydroxy-3-oxazolidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Boc-4-benzyl-5-chloromethyl-5-hydroxy-3-oxazolidine(291279-17-9)
    11. EPA Substance Registry System: N-Boc-4-benzyl-5-chloromethyl-5-hydroxy-3-oxazolidine(291279-17-9)

  • 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: 291279-17-9(Hazardous Substances Data)

291279-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 291279-17-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,1,2,7 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 291279-17:
(8*2)+(7*9)+(6*1)+(5*2)+(4*7)+(3*9)+(2*1)+(1*7)=159
159 % 10 = 9
So 291279-17-9 is a valid CAS Registry Number.

291279-17-9Relevant articles and documents

Practical synthesis of α-aminoalkyl-α′-chloromethylketone derivatives. Part 1: Chloromethylation of N-protected 3-oxazolidin-5-ones

Onishi, Tomoyuki,Hirose, Naoko,Nakano, Takashi,Nakazawa, Masakazu,Izawa, Kunisuke

, p. 5883 - 5885 (2001)

Reaction of N-protected 3-oxazolidin-5-ones with in situ-generated chloromethyllithium afforded N-protected 5-chloromethyl-5-hydroxy-3-oxazolidines without racemization. They were easily hydrolyzed to give α-aminoalkyl-α′-chloromethylketone derivatives, which are useful intermediates for several protease inhibitors.

Creation of an artificial metalloprotein with a Hoveyda-Grubbs catalyst moiety through the intrinsic inhibition mechanism of α-chymotrypsin

Matsuo, Takashi,Imai, Chie,Yoshida, Takefumi,Saito, Takashi,Hayashi, Takashi,Hirota, Shun

supporting information; experimental part, p. 1662 - 1664 (2012/03/27)

An l-phenylalanyl chloromethylketone-based inhibitor equipped with a Hoveyda-Grubbs catalyst moiety was regioselectively incorporated into the cleft of α-chymotrypsin through the intrinsic inhibition mechanism of the protein to construct an artificial organometallic protein. The Royal Society of Chemistry 2012.

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