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alpha-acetoxy-N-nitrosopiperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53198-44-0

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53198-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53198-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,9 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53198-44:
(7*5)+(6*3)+(5*1)+(4*9)+(3*8)+(2*4)+(1*4)=130
130 % 10 = 0
So 53198-44-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N2O3/c1-6(10)12-7-4-2-3-5-9(7)8-11/h7H,2-5H2,1H3

53198-44-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name α-acetyoxy-N-nitrosopiperidine

1.2 Other means of identification

Product number -
Other names α-acetoxy-N-nitrosopiperidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:53198-44-0 SDS

53198-44-0Downstream Products

53198-44-0Relevant academic research and scientific papers

Cyclic α-acetoxynitrosamines: Mechanisms of decomposition and stability of α-hydroxynitrosamine and nitrosiminium ion reactive intermediates

Chahoua, Latifa,Cai, Hongliang,Fishbein, James C.

, p. 5161 - 5169 (2007/10/03)

A study of the kinetics and mechanism of the decay of α-acetoxy-N- nitrosopyrrolidine and α-acetoxy-N-nitrosopiperidine are reported. The compounds differ in reactivity by more than 2 orders of magnitude at physiological pH. On the basis of thermodynamic

The Chemistry of Nitrosamines, IV. - Syntheses of α-C-Functionalized N-Nitrosodialkylamines: Esters and Ethers of 1-alcohols

Mueller, Eduard,Kettler, Regina,Wiessler, Manfred

, p. 1468 - 1493 (2007/10/02)

Imines (Schiff's bases) and nitrosyl chloride react to give N-alkyl-1-chloro-N-nitrosoalkylamines 13.Nucleophilic substitution by acetate or p-nitrobenzoate affords the acetates 7 and 9 and p-nitrobenzoates 8 and 10, respectively.The spectroscopic and chemical data of the newly synthesized compounds are discussed.

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