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3,4-Pyrrolidinediol, 2-(hydroxymethyl)-5-(4-nitrophenyl)-, (2R,3R,4S,5S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 3,4-Pyrrolidinediol, 2-(hydroxymethyl)-5-(4-nitrophenyl)-, (2R,3R,4S,5S)-

    Cas No: 188745-01-9

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  • 188745-01-9 Structure
  • Basic information

    1. Product Name: 3,4-Pyrrolidinediol, 2-(hydroxymethyl)-5-(4-nitrophenyl)-, (2R,3R,4S,5S)-
    2. Synonyms: 3,4-Pyrrolidinediol, 2-(hydroxymethyl)-5-(4-nitrophenyl)-, (2R,3R,4S,5S)-
    3. CAS NO:188745-01-9
    4. Molecular Formula: C11H14 N2 O5
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 188745-01-9.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: 3,4-Pyrrolidinediol, 2-(hydroxymethyl)-5-(4-nitrophenyl)-, (2R,3R,4S,5S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-Pyrrolidinediol, 2-(hydroxymethyl)-5-(4-nitrophenyl)-, (2R,3R,4S,5S)-(188745-01-9)
    11. EPA Substance Registry System: 3,4-Pyrrolidinediol, 2-(hydroxymethyl)-5-(4-nitrophenyl)-, (2R,3R,4S,5S)-(188745-01-9)
  • 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: 188745-01-9(Hazardous Substances Data)

188745-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 188745-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,7,4 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 188745-01:
(8*1)+(7*8)+(6*8)+(5*7)+(4*4)+(3*5)+(2*0)+(1*1)=179
179 % 10 = 9
So 188745-01-9 is a valid CAS Registry Number.

188745-01-9Downstream Products

188745-01-9Relevant articles and documents

Transition-state inhibitors for nucleoside hydrolase and transferase reactions

-

, (2008/06/13)

This invention is directed to transition-state analog compounds and to the use of said compounds as inhibitors of nucleoside hydrolase and transferase enzyme activity of parasites. This invention is further directed to the use of said compounds to treat infections and diseases caused by certain bacterial and plant toxins.

Synthesis of transition state inhibitors for N-riboside hydrolases and transferases

Furneaux, Richard H.,Limberg, Gerrit,Tyler, Peter C.,Schramm, Vern L.

, p. 2915 - 2930 (2007/10/03)

A number of 1,4-dideoxy-1,4-imino-1-(S)-(substituted phenyl)-D-ribitols bearing aromatic OH, NH2, NO2, CO2H and halogeno moieties, and a 3-pyridyl analogue have been synthesized. The key step is die condensation of aryllithium or aryl Grignard reagents with the imine 3; derived from the protected 1,4-dideoxy-1,4-imino-D-ribitol 4.

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