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208041-36-5

(R)-4-ALLYLOXAZOLIDIN-2-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 208041-36-5 Structure

  • Basic information

    1. Product Name: (R)-4-ALLYLOXAZOLIDIN-2-ONE
    2. Synonyms: (R)-4-ALLYLOXAZOLIDIN-2-ONE
    3. CAS NO:208041-36-5
    4. Molecular Formula: C6H9NO2
    5. Molecular Weight: 127.14
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 208041-36-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-4-ALLYLOXAZOLIDIN-2-ONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-4-ALLYLOXAZOLIDIN-2-ONE(208041-36-5)
    11. EPA Substance Registry System: (R)-4-ALLYLOXAZOLIDIN-2-ONE(208041-36-5)

  • 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: 208041-36-5(Hazardous Substances Data)

208041-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 208041-36-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,0,4 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 208041-36:
(8*2)+(7*0)+(6*8)+(5*0)+(4*4)+(3*1)+(2*3)+(1*6)=95
95 % 10 = 5
So 208041-36-5 is a valid CAS Registry Number.

208041-36-5Upstream product

208041-36-5Relevant articles and documents

Rational design of azepane-glycoside antibiotics targeting the bacterial ribosome

Barluenga, Sofia,Simonsen, Klaus B.,Littlefield, Ethel S.,Ayida, Benjamin K.,Vourloumis, Dionisios,Winters, Geoffrey C.,Takahashi, Masayuki,Shandrick, Sarah,Zhao, Qiang,Han, Qing,Hermann, Thomas

, p. 713 - 718 (2004)

RNA recognition by natural aminoglycoside antibiotics depends on the 2-deoxystreptamine (2-DOS) scaffold which participates in specific hydrogen bonds with the ribosomal decoding-site target. Three-dimensional structure information has been used for the design of azepane-monoglycosides, building blocks for novel antibiotics in which 2-DOS is replaced by a heterocyclic scaffold. Azepane-glycosides showed target binding and translation inhibition in the low micromolar range and inhibited growth of Staphylococcus aureus, including aminoglycoside-resistant strains.

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