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CAS

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1332828-02-0

(S)-[1-(2-methoxy-phenyl)-ethyl]pyridin-2-ylmethylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1332828-02-0 Structure

  • Basic information

    1. Product Name: (S)-[1-(2-methoxy-phenyl)-ethyl]pyridin-2-ylmethylamine
    2. Synonyms: (S)-[1-(2-methoxy-phenyl)-ethyl]pyridin-2-ylmethylamine
    3. CAS NO:1332828-02-0
    4. Molecular Formula:
    5. Molecular Weight: 242.321
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1332828-02-0.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)-[1-(2-methoxy-phenyl)-ethyl]pyridin-2-ylmethylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-[1-(2-methoxy-phenyl)-ethyl]pyridin-2-ylmethylamine(1332828-02-0)
    11. EPA Substance Registry System: (S)-[1-(2-methoxy-phenyl)-ethyl]pyridin-2-ylmethylamine(1332828-02-0)

  • 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: 1332828-02-0(Hazardous Substances Data)

1332828-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1332828-02-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,8,2 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1332828-02:
(9*1)+(8*3)+(7*3)+(6*2)+(5*8)+(4*2)+(3*8)+(2*0)+(1*2)=140
140 % 10 = 0
So 1332828-02-0 is a valid CAS Registry Number.

1332828-02-0Downstream Products

1332828-02-0Relevant articles and documents

AMINE DERIVATIVES AS POTASSIUM CHANNEL BLOCKERS

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Page/Page column 53; 66, (2015/09/10)

The present invention relates to compounds useful in the modulation of potassium channel activity in cells, in particular the activity of Kv1.3 channels found in T cells. The invention also relates to the use of these compounds in the treatment or prevention of autoimmune and inflammatory diseases, including multiple sclerosis, pharmaceutical compositions containing these compounds and methods for their preparation.

Sequential reductive amination-hydrogenolysis: A one-pot synthesis of challenging chiral primary amines

Nugent, Thomas C.,Negru, Daniela E.,El-Shazly, Mohamed,Hu, Dan,Sadiq, Abdul,Bibi, Ahtaram,Umar, M. Naveed

, p. 2085 - 2092 (2011/10/19)

Difficult-to-access chiral primary amines were formed in good to high yield and ee using a rare example of a one-pot synthesis from prochiral ketones (sequential reductive amination-hydrogenloysis). As a highlight we also demonstrate a one-pot reductive amination-hydrogenolysis-reductive amination (five reactions) of ortho-methoxyacetophenone resulting in the chiral diamine 1-(2-methoxyphenyl)ethyl-(2-pyridylmethyl)-amine (4) (58% overall yield, >99% ee), a new organocatalyst for aqueous enantioselective aldol reactions. Copyright

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