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2-Ethylpiperidine hydrochloride is a chemical compound with the molecular formula C7H16ClNO and a molecular weight of 157.66 g/mol. It is a white crystalline solid that is soluble in water and various organic solvents. 2-ETHYLPIPERIDINE HYDROCHLORIDE is primarily used as a pharmaceutical intermediate in the synthesis of various drugs, particularly those targeting the central nervous system. It is also employed in the production of agrochemicals and other specialty chemicals. Due to its potential health risks, including irritation to the eyes, skin, and respiratory system, it is essential to handle 2-ethylpiperidine hydrochloride with proper safety measures and personal protective equipment.

1484-99-7

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1484-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1484-99-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1484-99:
(6*1)+(5*4)+(4*8)+(3*4)+(2*9)+(1*9)=97
97 % 10 = 7
So 1484-99-7 is a valid CAS Registry Number.

1484-99-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylpiperidine,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-ethylpiperidine hydrochloride

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:1484-99-7 SDS

1484-99-7Downstream Products

1484-99-7Relevant academic research and scientific papers

Scalable and Straightforward Synthesis of All Isomeric (Cyclo)alkylpiperidines

Subota, Andrii I.,Lutsenko, Anton O.,Vashchenko, Bohdan V.,Volochnyuk, Dmitriy M.,Levchenko, Vitalina,Dmytriv, Yurii V.,Rusanov, Eduard B.,Gorlova, Alina O.,Ryabukhin, Sergey V.,Grygorenko, Oleksandr O.

, p. 3636 - 3648 (2019/06/13)

An efficient approach towards introducing (cyclo)alkyl substituents at C-2, C-3 or C-4 positions of the piperidine ring was described. The method relied on the straightforward two-step reaction sequence based on the formal sp3–sp3 re

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