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119204-13-6

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119204-13-6 Usage

Chemical structure

The compound has a piperidine backbone, a benzyl group, and a hydroxyethyl side chain.

Common use

It is commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds.

Pharmaceutical applications

The compound has potential pharmaceutical applications due to its ability to modulate the activity of neurotransmitters in the central nervous system.

Unique structure

Its unique structure makes it a valuable precursor in the development of medicinal drugs and research chemicals.

Field of application

1-BENZYL-2-(2-HYDROXYETHYL) PIPERIDINE has diverse potential applications in the field of medicinal chemistry and drug development.
It's worth noting that the material provided does not give specific information about the chemical properties of the compound, such as its molecular weight, solubility, or reactivity. Additionally, it does not provide any information about the synthesis methods or the specific pharmaceuticals or organic compounds that are synthesized using this compound as an intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 119204-13-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,2,0 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 119204-13:
(8*1)+(7*1)+(6*9)+(5*2)+(4*0)+(3*4)+(2*1)+(1*3)=96
96 % 10 = 6
So 119204-13-6 is a valid CAS Registry Number.

119204-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-benzylpiperidin-2-yl)ethanol

1.2 Other means of identification

Product number -
Other names 1-benzyl-2-piperidineethanol

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:119204-13-6 SDS

119204-13-6Relevant articles and documents

Cycloaddition of 2,3,4,5-Tetrahydropyridine N-Oxide to Vinyl Ethers. Enantioselective Synthesis of 2-(N-Benzylpiperidin-2-yl)ethanol

Carruthers, William,Coggins, Peter,Weston, John B.

, p. 117 - 118 (1991)

The title compound has been obtained in high optical purity by cycloaddition of 2,3,4,5-tetrahydropyridine N-oxide and (R)-2,2-dimethyl-1-phenylpropyl vinyl ether followed by N-benzylation and reduction of the salt with lithium aluminium hydride.

USE OF AMINOINDANE COMPOUNDS IN TREATING OVERACTIVE BLADDER AND INTERSTITIAL CYSTITIS

-

Page/Page column 132-133, (2014/03/22)

The present application provides methods of using the aminoindane compounds of formula (I) or (II) in treating an overactive bladder or interstitial cystitis by administering one or more of the compounds to a patient.

Electrooxidative cyclization of hydroxyamino compounds possessing a benzyl group

Okimoto, Mitsuhiro,Ohashi, Kousuke,Yamamori, Haruki,Nishikawa, Shinnosuke,Hoshi, Masayuki,Yoshida, Takashi

experimental part, p. 1315 - 1322 (2012/06/30)

Several novel 2-aryl-1,3-oxazinane and 2-aryl-1,3-oxazolidine derivatives were synthesized from N-benzyl-2-piperidineethanols and N-benzyl-2- piperidinemethanols, respectively, by using electrooxidative methods in methanol. For these reactions, the yields of the corresponding cyclized compounds were significantly increased by using catalytic amounts of iodide ions. In contrast, 3-dialkylamino-1-phenylpropanols afforded the expected cyclic 6-phenyl-1,3-oxazinane derivatives using only a small excess of base. Georg Thieme Verlag Stuttgart · New York.

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