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CAS

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112897-02-6

C23H25N2O4B is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 112897-02-6 Structure

  • Basic information

    1. Product Name: C23H25N2O4B
    2. Synonyms:
    3. CAS NO:112897-02-6
    4. Molecular Formula:
    5. Molecular Weight: 404.273
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112897-02-6.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: C23H25N2O4B(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23H25N2O4B(112897-02-6)
    11. EPA Substance Registry System: C23H25N2O4B(112897-02-6)

  • 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: 112897-02-6(Hazardous Substances Data)

112897-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112897-02-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,8,9 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112897-02:
(8*1)+(7*1)+(6*2)+(5*8)+(4*9)+(3*7)+(2*0)+(1*2)=126
126 % 10 = 6
So 112897-02-6 is a valid CAS Registry Number.

112897-02-6Downstream Products

112897-02-6Relevant articles and documents

N,N'-Dibenzyl-N,N'-ethylenetartramide: A Rationally Designed Chiral Auxiliary for the Allylboration Reaction

Roush, William R.,Banfi, Luca

, p. 3979 - 3982 (1988)

The chiral auxiliary designated in the title was designed as a probe of our previously suggested mechnism of asymmetric induction with tartrate allylboronates 1-3, namely that n/n electronic repulsive interactions between electron pairs on the aldehydic oxygen atom and an ester carbonyl disfavor transition-state C relative to A.The results reported for the new reagent 5 strongly support this thesis and suggest that the convergence of functional groups toward a metal center can be an exceedingly useful strategy for achieving a topological bias in the enantioselective functionalization of a carbonyl group.

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