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955036-36-9

tert-butyl 3-(4-methoxyphenyl)-2-oxopropylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 955036-36-9 Structure

  • Basic information

    1. Product Name: tert-butyl 3-(4-methoxyphenyl)-2-oxopropylcarbamate
    2. Synonyms: tert-butyl 3-(4-methoxyphenyl)-2-oxopropylcarbamate
    3. CAS NO:955036-36-9
    4. Molecular Formula:
    5. Molecular Weight: 279.336
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 955036-36-9.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: tert-butyl 3-(4-methoxyphenyl)-2-oxopropylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl 3-(4-methoxyphenyl)-2-oxopropylcarbamate(955036-36-9)
    11. EPA Substance Registry System: tert-butyl 3-(4-methoxyphenyl)-2-oxopropylcarbamate(955036-36-9)

  • 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: 955036-36-9(Hazardous Substances Data)

955036-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 955036-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,5,0,3 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 955036-36:
(8*9)+(7*5)+(6*5)+(5*0)+(4*3)+(3*6)+(2*3)+(1*6)=179
179 % 10 = 9
So 955036-36-9 is a valid CAS Registry Number.

955036-36-9Upstream product

955036-36-9Downstream Products

955036-36-9Relevant articles and documents

Synthesis of 2-Aminoazoles from Thioesters via α-Heterosubstituted Ketones by Copper-Mediated Cross-Coupling

Kobayashi, Hiroyuki,Eickhoff, John A.,Zakarian, Armen

, p. 9989 - 9999 (2015)

Facile synthesis of a variety of α-heterosubstituted ketones under mild conditions was achieved by copper-mediated cross-coupling of thioesters with functionalized organostannanes. Application of this coupling methodology provided a concise pathway for the conversion of carboxylic acids to 2-aminoimidazoles, 2-aminothiazoles, and 2-aminooxazoles via thioesters in practical yields.

Inhibitors of semicarbazide-sensitive amine oxidase (SSAO) and VAP-1 mediated adhesion useful for treatment and prevention of diseases

-

Page/Page column 56, (2008/06/13)

Compositions and methods of using compositions for treatment of inflammatory diseases and immune disorders are provided. Allylamino compounds are disclosed which are inhibitors of semicarbazide-sensitive amine oxidase (SSAO) and/or vascular adhesion protein 1 (VAP-1). The compounds have therapeutic utility in suppressing inflammation and inflammatory responses, and in treatment of several disorders, including multiple sclerosis and stroke.

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