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CAS

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61533-06-0

Piperidinium, 1-(2-methoxy-2-oxoethyl)-1-(phenylmethyl)-, bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 61533-06-0 Structure

  • Basic information

    1. Product Name: Piperidinium, 1-(2-methoxy-2-oxoethyl)-1-(phenylmethyl)-, bromide
    2. Synonyms:
    3. CAS NO:61533-06-0
    4. Molecular Formula: C15H22NO2.Br
    5. Molecular Weight: 328.249
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 61533-06-0.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: Piperidinium, 1-(2-methoxy-2-oxoethyl)-1-(phenylmethyl)-, bromide(CAS DataBase Reference)
    10. NIST Chemistry Reference: Piperidinium, 1-(2-methoxy-2-oxoethyl)-1-(phenylmethyl)-, bromide(61533-06-0)
    11. EPA Substance Registry System: Piperidinium, 1-(2-methoxy-2-oxoethyl)-1-(phenylmethyl)-, bromide(61533-06-0)

  • 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: 61533-06-0(Hazardous Substances Data)

61533-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61533-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,3 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61533-06:
(7*6)+(6*1)+(5*5)+(4*3)+(3*3)+(2*0)+(1*6)=100
100 % 10 = 0
So 61533-06-0 is a valid CAS Registry Number.

61533-06-0Relevant articles and documents

A formal method for the de-N,N-dialkylation of Sommelet-Hauser rearrangement products

Tayama, Eiji,Sato, Ryota,Takedachi, Keisuke,Iwamoto, Hajime,Hasegawa, Eietsu

, p. 4710 - 4718 (2012/07/28)

Selective amine de-alkylation enables the conversion of Sommelet-Hauser rearrangement products into 2-aryl-2-bromoacetic acid derivatives. These compounds are valuable synthetic intermediates in the synthesis of α-aryl-α-amino or α-aryl-β-amino acid deriv

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