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(S,Z)-2-benzhydryl-5-(2-mesitylhydrazono)pyrrolidine hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1447823-10-0 Structure
  • Basic information

    1. Product Name: (S,Z)-2-benzhydryl-5-(2-mesitylhydrazono)pyrrolidine hydrochloride
    2. Synonyms:
    3. CAS NO:1447823-10-0
    4. Molecular Formula:
    5. Molecular Weight: 419.997
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1447823-10-0.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: (S,Z)-2-benzhydryl-5-(2-mesitylhydrazono)pyrrolidine hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S,Z)-2-benzhydryl-5-(2-mesitylhydrazono)pyrrolidine hydrochloride(1447823-10-0)
    11. EPA Substance Registry System: (S,Z)-2-benzhydryl-5-(2-mesitylhydrazono)pyrrolidine hydrochloride(1447823-10-0)
  • 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: 1447823-10-0(Hazardous Substances Data)

1447823-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1447823-10-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,7,8,2 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1447823-10:
(9*1)+(8*4)+(7*4)+(6*7)+(5*8)+(4*2)+(3*3)+(2*1)+(1*0)=170
170 % 10 = 0
So 1447823-10-0 is a valid CAS Registry Number.

1447823-10-0Relevant articles and documents

Highly enantioselective intermolecular stetter reaction of simple acrylates: Synthesis of α-chiral γ-Ketoesters

Wurz, Nathalie E.,Daniliuc, Constantin G.,Glorius, Frank

, p. 16297 - 16301 (2013/02/22)

Simple Stetter: A novel N-heterocyclic carbene (NHC) was designed by combining an electron-rich 2,6-dimethoxy substituent and an underestimated yet promising chiral motif. With this NHC in hand, a highly enantioselective intermolecular Stetter reaction of simple acrylates was developed, yielding versatile α-chiral γ-ketoesters. This represents the first catalytic asymmetric route towards these valuable compounds (see scheme).

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