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201666-47-9

(5-amino-2-nitro-phenyl)-imidazol-1-yl-methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 201666-47-9 Structure

  • Basic information

    1. Product Name: (5-amino-2-nitro-phenyl)-imidazol-1-yl-methanone
    2. Synonyms: (5-amino-2-nitro-phenyl)-imidazol-1-yl-methanone
    3. CAS NO:201666-47-9
    4. Molecular Formula:
    5. Molecular Weight: 232.199
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 201666-47-9.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: (5-amino-2-nitro-phenyl)-imidazol-1-yl-methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5-amino-2-nitro-phenyl)-imidazol-1-yl-methanone(201666-47-9)
    11. EPA Substance Registry System: (5-amino-2-nitro-phenyl)-imidazol-1-yl-methanone(201666-47-9)

  • 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: 201666-47-9(Hazardous Substances Data)

201666-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201666-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,6,6 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 201666-47:
(8*2)+(7*0)+(6*1)+(5*6)+(4*6)+(3*6)+(2*4)+(1*7)=109
109 % 10 = 9
So 201666-47-9 is a valid CAS Registry Number.

201666-47-9Relevant articles and documents

Moenomycin A: New chemistry that allows to attach the antibiotic to reporter groups, solid supports, and proteins

Kempin, Uwe,Hennig, Lothar,Knoll, Dietmar,Welzel, Peter,Mueller, Dietrich,Markus, Astrid,Van Heijenoort, Jean

, p. 17669 - 17690 (1997)

Moenomycin A (18) on reaction with the diazonium salt derived from bifunctional (protected) 15 yields the coupling product 19 which on reduction is converted into the moenomycin thiol derivative 21. Thiol 21 has been used to prepare selectively moenomycin dansyl and biotin adducts 26 and 28, respectively. This work was performed with the aim to use moenomycin as a tool for studies of the transglycosylation step in peptidoglycan biosynthesis.

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