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CAS

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615569-04-5

(1R,3R,4R)-3-hydroxy-4-tert-butoxycarbonylamino-cyclohexanecarboxylic acid amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 615569-04-5 Structure

  • Basic information

    1. Product Name: (1R,3R,4R)-3-hydroxy-4-tert-butoxycarbonylamino-cyclohexanecarboxylic acid amide
    2. Synonyms: (1R,3R,4R)-3-hydroxy-4-tert-butoxycarbonylamino-cyclohexanecarboxylic acid amide
    3. CAS NO:615569-04-5
    4. Molecular Formula:
    5. Molecular Weight: 258.318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 615569-04-5.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: (1R,3R,4R)-3-hydroxy-4-tert-butoxycarbonylamino-cyclohexanecarboxylic acid amide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,3R,4R)-3-hydroxy-4-tert-butoxycarbonylamino-cyclohexanecarboxylic acid amide(615569-04-5)
    11. EPA Substance Registry System: (1R,3R,4R)-3-hydroxy-4-tert-butoxycarbonylamino-cyclohexanecarboxylic acid amide(615569-04-5)

  • 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: 615569-04-5(Hazardous Substances Data)

615569-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 615569-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,5,5,6 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 615569-04:
(8*6)+(7*1)+(6*5)+(5*5)+(4*6)+(3*9)+(2*0)+(1*4)=165
165 % 10 = 5
So 615569-04-5 is a valid CAS Registry Number.

615569-04-5Relevant articles and documents

Novel cyclohexyl-amides as potent antibacterials targeting bacterial type IIA topoisomerases

Miles, Timothy J.,Barfoot, Christopher,Brooks, Gerald,Brown, Pamela,Chen, Dongzhao,Dabbs, Steven,Davies, David T.,Downie, David L.,Eyrisch, Susanne,Giordano, Ilaria,Gwynn, Michael N.,Hennessy, Alan,Hoover, Jennifer,Huang, Jianzhong,Jones, Graham,Markwell, Roger,Rittenhouse, Stephen,Xiang, Hong,Pearson, Neil

, p. 7483 - 7488 (2012/02/04)

As part of our wider efforts to exploit novel mode of action antibacterials, we have discovered a series of cyclohexyl-amide compounds that has good Gram positive and Gram negative potency. The mechanism of action is via inhibition of bacterial topoisomer

ANTIBACTERIAL COMPOUNDS

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Page 58; 59, (2008/06/13)

Cyclohexane and cyclohexene derivatives and pharmaceutically acceptable derivatives thereof useful in methods of treatment of bacterial infections in mammals, particularly man

NITROGEN-CONTAINING BICYCLIC HETEROCYCLES FOR USE AS ANTIBACTERIALS

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Page/Page column 123, (2010/02/07)

Cyclohexane and cyclohexene derivatives and pharmaceutically acceptable derivatives hereof useful in methods of treatment of bacterial infections in mammals, particularly man.

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