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CAS

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1597586-15-6

(S)-1-benzyl-2-(methoxydi-p-tolylmethyl)pyrrolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1597586-15-6 Structure

  • Basic information

    1. Product Name: (S)-1-benzyl-2-(methoxydi-p-tolylmethyl)pyrrolidine
    2. Synonyms: (S)-1-benzyl-2-(methoxydi-p-tolylmethyl)pyrrolidine
    3. CAS NO:1597586-15-6
    4. Molecular Formula:
    5. Molecular Weight: 385.549
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1597586-15-6.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: (S)-1-benzyl-2-(methoxydi-p-tolylmethyl)pyrrolidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-1-benzyl-2-(methoxydi-p-tolylmethyl)pyrrolidine(1597586-15-6)
    11. EPA Substance Registry System: (S)-1-benzyl-2-(methoxydi-p-tolylmethyl)pyrrolidine(1597586-15-6)

  • 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: 1597586-15-6(Hazardous Substances Data)

1597586-15-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1597586-15-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,9,7,5,8 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1597586-15:
(9*1)+(8*5)+(7*9)+(6*7)+(5*5)+(4*8)+(3*6)+(2*1)+(1*5)=236
236 % 10 = 6
So 1597586-15-6 is a valid CAS Registry Number.

1597586-15-6Relevant articles and documents

Enantioselective copper(I/II)-catalyzed conjugate addition of nitro esters to β,γ-unsaturated α-ketoesters

Zhang, Sheng,Xu, Kun,Guo, Fengfeng,Hu, Yanbin,Zha, Zhenggen,Wang, Zhiyong

, p. 979 - 982 (2014)

A highly enantioselective Michael addition of nitroacetates to β,γ-unsaturated α-ketoesters was developed by using chiral copper catalysts. The Michael addition products can be obtained in high yields with up to 99 % ee. With these densely functionalized products, the chiral cyclic nitrones, which are important synthetic intermediates, can be obtained in one step. Copyright

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