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[4-(2-AMINO-ETHYL)-PHENYL]-METHANOL HYDROCHLORIDE is a chemical compound characterized by the presence of an aminoethyl group attached to a phenyl ring, along with a methanol group and a hydrochloride ion. This structure endows it with potential for a broad spectrum of biological activities, making it a valuable compound in the fields of chemical research and pharmaceutical applications.

68559-71-7

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68559-71-7 Usage

Uses

Used in Chemical Research:
[4-(2-AMINO-ETHYL)-PHENYL]-METHANOL HYDROCHLORIDE is used as a research compound for exploring its chemical properties and potential interactions with other molecules. Its unique structure allows scientists to study various biochemical processes and mechanisms.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, [4-(2-AMINO-ETHYL)-PHENYL]-METHANOL HYDROCHLORIDE is used as a starting material or intermediate in the synthesis of new drugs. Its versatile structure can be modified to create compounds with specific therapeutic properties.
Used in the Development of New Drugs:
[4-(2-AMINO-ETHYL)-PHENYL]-METHANOL HYDROCHLORIDE is used as a key component in the development of new drugs due to its potential for a wide range of biological activities. Its specific properties and potential uses may vary depending on the context in which it is being studied or utilized, making it a promising candidate for various therapeutic applications.
Used in the Study of Neurotransmitters:
[4-(2-AMINO-ETHYL)-PHENYL]-METHANOL HYDROCHLORIDE is used as a research tool for investigating the role of neurotransmitters and other biochemical processes in the body. Its structure may allow for the development of compounds that can modulate neurotransmitter activity, potentially leading to treatments for neurological disorders.
Used in Biochemical Process Research:
In the field of biochemistry, [4-(2-AMINO-ETHYL)-PHENYL]-METHANOL HYDROCHLORIDE is used as a compound of interest for studying various cellular and molecular processes. Its unique structure may provide insights into the mechanisms underlying certain biological functions and contribute to the development of targeted therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 68559-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,5,5 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 68559-71:
(7*6)+(6*8)+(5*5)+(4*5)+(3*9)+(2*7)+(1*1)=177
177 % 10 = 7
So 68559-71-7 is a valid CAS Registry Number.

68559-71-7 Well-known Company Product Price

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  • Aldrich

  • (JWP00136)  [4-(2-Amino-ethyl)-phenyl]-methanol hydrochloride  AldrichCPR

  • 68559-71-7

  • JWP00136-1G

  • 3,866.85CNY

  • Detail

68559-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-aminoethyl)-benzyl alcohol hydrochloride

1.2 Other means of identification

Product number -
Other names 4-(2-AMINO-ETHYL)-PHENYL-METHANOL 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:68559-71-7 SDS

68559-71-7Relevant academic research and scientific papers

A traceless photocleavable linker for the automated glycan assembly of carbohydrates with free reducing ends

Wilsdorf,Schmidt,Bartetzko,Dallabernardina,Schuhmacher,Seeberger,Pfrengle

supporting information, p. 10187 - 10189 (2016/08/18)

We report a traceless photocleavable linker for the automated glycan assembly of carbohydrates with free reducing ends. The reductive-labile functionality in the linker tolerates all commonly used reagents and protocols for automated glycan assembly, as demonstrated with the successful preparation of nine plant cell wall-related oligosaccharides, and is cleaved by hydrogenolysis.

Hypoglycaemically and hypolipidaemically effective n-substituted carboxylic acid amides

-

, (2008/06/13)

An N-substituted carboxylic acid amide of the formula STR1 wherein A is a valency bond or an oxygen or sulphur atom or a methylene, ethylene, vinylene, ethyleneoxa or ethylenethia radical, V is a trivalent hydrocarbon radical containing up to 4 carbon ato

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