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4-(Aminomethyl)-1-methyl-piperidin-4-ol is a chemical compound characterized by its molecular weight of 144.21 g/mol and its appearance as a white to off-white solid. It belongs to the class of piperidine derivatives, which are organic compounds with a five-membered ring containing one nitrogen atom. 4-(Aminomethyl)-1-methyl-piperidin-4-ol's structure includes both amine and alcohol functional groups, along with the piperidinyl ring, which contribute to its diverse applications in chemical synthesis and pharmaceuticals. However, it is important to handle 4-(Aminomethyl)-1-methyl-piperidin-4-ol with caution due to its potential to cause skin and eye irritation, and the need for further evaluation of its safety in human health and the environment.

26228-68-2

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26228-68-2 Usage

Uses

Used in Chemical Synthesis:
4-(Aminomethyl)-1-methyl-piperidin-4-ol is used as a building block in chemical synthesis for its versatile functional groups, which allow for the creation of various chemical compounds and intermediates.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, 4-(Aminomethyl)-1-methyl-piperidin-4-ol is utilized as a key component in the development of new drugs. Its unique structure and functional groups enable it to be incorporated into medicinal compounds, potentially leading to the discovery of novel therapeutic agents.
Used in Research and Development:
4-(Aminomethyl)-1-methyl-piperidin-4-ol is employed as a research tool in the field of organic chemistry and medicinal chemistry. Its properties and reactivity are studied to gain insights into the synthesis of new compounds and to understand the underlying chemical reactions.
Used in Material Science:
Although not explicitly mentioned in the provided materials, the compound's structural features may also find applications in material science, where its amine and alcohol groups could be utilized in the development of new materials with specific properties, such as polymers or coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 26228-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,2 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 26228-68:
(7*2)+(6*6)+(5*2)+(4*2)+(3*8)+(2*6)+(1*8)=112
112 % 10 = 2
So 26228-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H16N2O/c1-9-4-2-7(10,6-8)3-5-9/h10H,2-6,8H2,1H3

26228-68-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(aminomethyl)-1-methylpiperidin-4-ol

1.2 Other means of identification

Product number -
Other names 4-aminomethyl-4-hydroxy-1-methylpiperidine

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:26228-68-2 SDS

26228-68-2Relevant academic research and scientific papers

Histone Deacetylase Inhibitors and Methods of Use Thereof

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Paragraph 0242; 0243, (2019/09/16)

The present invention relates to methods of modulating activity of histone deacetylases (HDACs). The present invention also relates to methods of treating HDAC-associated diseases including, but not limited to, cancers, inflammatory disorders, and neurodegenerative disorders. The present invention also provides novel compounds and compositions thereof and methods of preparation of the same. The present invention also includes methods of inhibiting HDACs, and methods of treating HDAC-associated diseases using the compounds of the invention.

Substituted imidazo[1,2-b]pyridazines as protein kinase inhibitors

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Page/Page column 139, (2016/09/13)

The present invention provides protein kinase having one of the following structures (I), (II) or (III): or a stereoisomer, prodrug, tautomer or pharmaceutically acceptable salt thereof, wherein R, R1, R2 and X are as defined herein. Compositions and methods for using the same in the treatment of cancer, autoimmune, inflammatory and other Pim kinase-associated conditions are also disclosed.

QUINOLONE DERIVATIVES AS FIBROBLAST GROWTH FACTOR INHIBITORS

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Page/Page column 124, (2014/12/09)

Compounds of formula (Ι') that are Fibroblast Growth Factor Inhibitors (FGFR) and are therefore useful for the treatment of diseases treatable by inhibition of FGFR are disclosed. Also disclosed are pharmaceutical compositions containing such compounds and processes for preparing such compounds.

HETEROCYCLIC PROTEIN KINASE INHIBITORS

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Paragraph 00329, (2013/03/26)

The present invention provides protein kinase having one of the following structures (I), (II) or (III): or a stereoisomer, prodrug, tautomer or pharmaceutically acceptable salt thereof, wherein R, R1, R2 and X are as defined herein. Compositions and methods for using the same in the treatment of cancer, autoimmune, inflammatory and other Pim kinase-associated conditions are also disclosed.

Pyrrolo [3,2-C] Pyridine-4-One 2-Indolinone Protein Kinase Inhibitors

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Page/Page column 93, (2010/02/16)

The present invention relates to pyrrolo[3,2-c]pyridine-4-one 2-indolinone compounds of Formula (I) and their pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R6, R7, R8X, Y and have the meaning cited in the specification.

PYRROLO [3,2-C] PYRIDINE-4-ONE 2-INDOLINONE PROTEIN KINASE INHIBITORS

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Page/Page column 155-156, (2010/11/28)

The present invention relates to pyrrolo[3,2-c]pyridine-4-one 2-indolinone compounds of Formula (I) and their pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R6, R7, R8 X , Y and …. have the meaning cited in the specifica

SUBSTITUTED IMIDAZOQUINOLINES, IMIDAZOPYRIDINES, AND IMIDAZONAPHTHYRIDINES

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Page/Page column 224, (2010/10/20)

Imidazo-quinoline, -pyridine, and -naphthyridine ring systems (particularly quinolines, tetrahydroquinolines, pyridines, [1,5]naphthyridines, [1,5]tetrahydronaphthyridines) substituted at the 1-position with a cyclic substituent, pharmaceutical compositions containing the compounds, methods of making these compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

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