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Piperidine, 1-(3-bromopropyl)-, hydrobromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58689-34-2

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58689-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58689-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,8 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58689-34:
(7*5)+(6*8)+(5*6)+(4*8)+(3*9)+(2*3)+(1*4)=182
182 % 10 = 2
So 58689-34-2 is a valid CAS Registry Number.

58689-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-bromopropyl)piperidine,hydrobromide

1.2 Other means of identification

Product number -
Other names 1-(3-Brom-propyl)-piperidin,Hydrobromid

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:58689-34-2 SDS

58689-34-2Relevant academic research and scientific papers

PYRAZOLO[1,5-A]PYRIDINES AND THEIR USE IN CANCER THERAPY

-

Page/Page column 84, (2009/03/07)

Pyrazolo[1,5-a]pyridines are described, including methods for their preparation, and their use as agents or drugs for cancer therapy, both alone or in combination with radiation and/or other anticancer drugs.

Electrooxidative cyclization of hydroquinolyl alcohols, hydroquinolylamines, and dimethyl aminomalonates

Okimoto, Mitsuhiro,Yoshida, Takashi,Hoshi, Masayuki,Hattori, Kazuyuki,Komata, Masashi,Numata, Kaori,Tomozawa, Kenta

, p. 236 - 242 (2008/02/11)

Several hydroquinolyl alcohols and amines were electrochemically oxidized in methanol in the presence of sodium methoxide and potassium iodide to afford the corresponding intramolecular cyclization products. Furthermore, several amino malonates were electrochemically oxidized to yield the corresponding heterocyclic compounds through an intramolecular carbon-carbon bond formation in the presence of sodium cyanide in methanol. CSIRO 2007.

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