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  • 1105738-88-2 Structure
  • Basic information

    1. Product Name: C17H17NO6S
    2. Synonyms:
    3. CAS NO:1105738-88-2
    4. Molecular Formula:
    5. Molecular Weight: 363.391
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1105738-88-2.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: C17H17NO6S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H17NO6S(1105738-88-2)
    11. EPA Substance Registry System: C17H17NO6S(1105738-88-2)
  • 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: 1105738-88-2(Hazardous Substances Data)

1105738-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1105738-88-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,5,7,3 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1105738-88:
(9*1)+(8*1)+(7*0)+(6*5)+(5*7)+(4*3)+(3*8)+(2*8)+(1*8)=142
142 % 10 = 2
So 1105738-88-2 is a valid CAS Registry Number.

1105738-88-2Downstream Products

1105738-88-2Relevant articles and documents

Substituent effects on the electrophilic activity of nitroarenes in reactions with carbanions

Blazej, Sylwia,Makosza, Mieczyslaw

supporting information; experimental part, p. 11113 - 11122 (2009/11/30)

The effect on electrophilic activity of substituents located para, ortho, and meta to the nitro group of nitrobenzenes was determined by using vicarious nucleophilic substitution of hydrogen (VNS) with the carbanion of chloromethyl phenyl sulfone (1) as the model process. Values for the relative activities of substituted nitroarenes are given relative to nitrobenzene, which was taken as the standard. This process was chosen as a model reaction because it meets key criteria, such as the wide range of substituents that can be present on the nitrobenzene ring, a low sensitivity to steric hindrance, and in particular the possibility of ensuring conditions in which the overall relative rates of reaction in competitive experiments are equal to the relative rates of nucleophilic addition. The values of relative rates of addition, which were taken to be a measure of electrophilic activity, were determined by competitive experiments in which pairs of nitroarenes competed for the VNS reaction with carbanion of 1. A comprehensive set of data for effects of substituents on the electrophilic activity of nitroarenes is presented for the first time.

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