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CAS

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314772-53-7

Propanoic acid, 2-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 314772-53-7 Structure

  • Basic information

    1. Product Name: Propanoic acid, 2-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-, ethyl ester
    2. Synonyms:
    3. CAS NO:314772-53-7
    4. Molecular Formula: C14H27NO3
    5. Molecular Weight: 257.373
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 314772-53-7.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: Propanoic acid, 2-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Propanoic acid, 2-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-, ethyl ester(314772-53-7)
    11. EPA Substance Registry System: Propanoic acid, 2-[(2,2,6,6-tetramethyl-1-piperidinyl)oxy]-, ethyl ester(314772-53-7)

  • 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: 314772-53-7(Hazardous Substances Data)

314772-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 314772-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,4,7,7 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 314772-53:
(8*3)+(7*1)+(6*4)+(5*7)+(4*7)+(3*2)+(2*5)+(1*3)=137
137 % 10 = 7
So 314772-53-7 is a valid CAS Registry Number.

314772-53-7Downstream Products

314772-53-7Relevant articles and documents

Organic Dye-Catalyzed Intermolecular Radical Coupling of α-Bromocarbonyls with Olefins: Photocatalytic Synthesis of 1,4-Ketocarbonyls Using Air as an Oxidant

Roy Chowdhury, Soumyadeep,Singh, Deepak,Hoque, Injamam Ul,Maity, Soumitra

, p. 13939 - 13950 (2020)

An organic dye-catalyzed visible light-promoted ketocarbonylation protocol of vinyl arenes has been disclosed with the help of α-bromocarbonyls where aerial oxygen played a role of an oxidant to install the keto-oxygen functionality. This unique process i

Radical mechanism in the elimination of 2-arylsulfinyl esters

Latorre, Antonio,Lopez, Irakusne,Ramirez, Victoria,Rodriguez, Santiago,Izquierdo, Javier,Gonzalez, Florenci V.,Vicent, Cristian

experimental part, p. 5191 - 5197 (2012/07/27)

The mechanism of the dehydrosulfenylation of 2-arylsulfinyl esters was investigated. The reaction was found to follow a homolytic cleavage mechanism as verified by electrospray ionization tandem mass spectrometry and experimental work. Rearranged sulfoxides are obtained as byproduct during the elimination reaction.

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