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CAS

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1562404-12-9

methyl (S)-2-methylene-3-(phenylamino)pentanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1562404-12-9 Structure

  • Basic information

    1. Product Name: methyl (S)-2-methylene-3-(phenylamino)pentanoate
    2. Synonyms: methyl (S)-2-methylene-3-(phenylamino)pentanoate
    3. CAS NO:1562404-12-9
    4. Molecular Formula:
    5. Molecular Weight: 219.283
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1562404-12-9.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: methyl (S)-2-methylene-3-(phenylamino)pentanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (S)-2-methylene-3-(phenylamino)pentanoate(1562404-12-9)
    11. EPA Substance Registry System: methyl (S)-2-methylene-3-(phenylamino)pentanoate(1562404-12-9)

  • 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: 1562404-12-9(Hazardous Substances Data)

1562404-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1562404-12-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,2,4,0 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1562404-12:
(9*1)+(8*5)+(7*6)+(6*2)+(5*4)+(4*0)+(3*4)+(2*1)+(1*2)=139
139 % 10 = 9
So 1562404-12-9 is a valid CAS Registry Number.

1562404-12-9Downstream Products

1562404-12-9Relevant articles and documents

METHOD OF PRODUCING CHIRAL N-SUBSTITUTED ALLYLIC AMINE COMPOUNDS

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Paragraph 0035, (2014/03/21)

The method relates to the field of asymmetric allylic amination and comprises preparing a chiral N-substituted allylic amine compound from the corresponding allylic substrates and substituted hydroxylamines, in the presence of a catalyst, said catalyst comprising copper compounds and a chiral ligand. Examples of chiral amine compounds which can be made using the method include Vigabatrin, Ezetimibe Terbinafme, Naftifme 3-methylmorphine, Sertraline, Cinacalcet, Mefloquine hydrochloride, and Rivastigmine. There are over 20,000 known bioactive molecules with chiral N-substituted allylic amine substructure. The method may also be used to produce non-natural chiral B-aminoacid esters, a sub-class of chiral N-substituted allylic amine compounds. Examples of B-aminoacid ester which can be produced by the disclosed method, include, but are not limited to, N-(2-methylpent-l-en-3-yl)benzenamine and Ethyl 2-methylene-3-(phenylamino)butanoate. Further, the products of the method described herein can be used to produce chiral heterocycles and bioactive molecules or materials.

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