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478082-32-5

Carbamic acid, ethyl(4-methoxyphenyl)-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 478082-32-5 Structure

  • Basic information

    1. Product Name: Carbamic acid, ethyl(4-methoxyphenyl)-, phenylmethyl ester
    2. Synonyms:
    3. CAS NO:478082-32-5
    4. Molecular Formula: C17H19NO3
    5. Molecular Weight: 285.343
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 478082-32-5.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: Carbamic acid, ethyl(4-methoxyphenyl)-, phenylmethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, ethyl(4-methoxyphenyl)-, phenylmethyl ester(478082-32-5)
    11. EPA Substance Registry System: Carbamic acid, ethyl(4-methoxyphenyl)-, phenylmethyl ester(478082-32-5)

  • 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: 478082-32-5(Hazardous Substances Data)

478082-32-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 478082-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,0,8 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 478082-32:
(8*4)+(7*7)+(6*8)+(5*0)+(4*8)+(3*2)+(2*3)+(1*2)=175
175 % 10 = 5
So 478082-32-5 is a valid CAS Registry Number.

478082-32-5Downstream Products

478082-32-5Relevant articles and documents

Iminomalonate as a convenient electrophilic amination reagent for grignard reagents

Niwa, Yasuki,Takayama, Kazuki,Shimizu, Makoto

, p. 1819 - 1825 (2002)

Diethyl 2-[N-(p-methoxyphenyl)imino]malonate underwent amination reactions with alkyl Grignard reagents to give N-aklylation products in good yields. The obtained N-alkylation products were readily converted into N-alkyl-panisidines by the oxidative removal of the malonate moiety. The p-methoxyphenyl group was subsequently deprotected to give primary amines.

Conjugated imines and iminium salts as versatile acceptors of nucleophiles

Shimizu, Makoto,Hachiya, Iwao,Mizota, Isao

scheme or table, p. 874 - 889 (2009/07/10)

Growing interests in nitrogen-containing molecules involving bioactive and functional materials have stimulated the recent development of synthetic methodologies where nucleophilic addition reactions to imino carbons are utilized in crucial steps. This article summarizes double nucleophilic addition reactions with α,β-unsaturated aldimines, addition reactions using alkynyl imines, "umpoled" reactions of α-imino esters, and the use of iminium salts as reactive electrophiles. The Royal Society of Chemistry 2009.

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