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4-(Chloromethyl)piperidine hydrochloride is an organic compound with the chemical formula C6H11Cl2N. It is a white crystalline solid that is soluble in water and serves as an important intermediate in the synthesis of various pharmaceutical compounds.

1822-61-3

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1822-61-3 Usage

Uses

Used in Pharmaceutical Industry:
4-(Chloromethyl)piperidine hydrochloride is used as a synthetic reagent for the production of N-type calcium channel blocker (NP118809) derivatives. These derivatives are essential in the development of medications that help regulate calcium ion flow in cells, which can be beneficial for treating conditions such as hypertension, angina, and certain heart arrhythmias.

Check Digit Verification of cas no

The CAS Registry Mumber 1822-61-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1822-61:
(6*1)+(5*8)+(4*2)+(3*2)+(2*6)+(1*1)=73
73 % 10 = 3
So 1822-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H12ClN/c7-5-6-1-3-8-4-2-6/h6,8H,1-5H2

1822-61-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(chloromethyl)piperidine,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-Chloromethyl-piperidine 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:1822-61-3 SDS

1822-61-3Upstream product

1822-61-3Downstream Products

1822-61-3Relevant academic research and scientific papers

Antipicornaviral pyridazinamines

-

, (2008/06/13)

Piperidinyl, pyrrolidinyl, azepinyl and piperazinyl pyridazines of formula STR1 wherein one or two carbon atoms of the STR2 moiety may be substituted with C1-4 alkyl, C1-4 alkyloxy or two carbon atoms of the CH2 groups of said moiety may be bridged with a C2-4 alkanediyl radical; X represents CH or N; R1 represents hydrogen, C1-4 alkyl, halo, hydroxy, trifluoromethyl, cyano, C1-4 alkyloxy, C1-4 alkylthio, C1-4 alkylsulfinyl, C1-4 alkylsulfonyl, C1-4 alkyloxycarbonyl, C1-4 alkylcarbonyl or aryl; R2 and R3 each independently represent hydrogen or C1-4 alkyl; Alk represents C1-4 alkanediyl; R4 and R5 each independently represent hydrogen, C1-4 alkyl or halo; and Het represents STR3 the addition salts and stereochemically isomeric forms thereof, said compounds having antipicornaviral activity. Pharmaceutical compositions containing these compounds as active ingredient, and a method of preparing said compounds and pharmaceutical compositions.

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