What is the 4-Piperidinol,1-methyl-?

4-Piperidinol,1-methyl- is clear colorless to yellowish liquid after melting, while it's Molecular Formula is C6H13NO. clear colorless to yellowish liquid after melting 4-Hydroxy-1-methylpiperidine is used as reactant for optimization of Novobiocin scaffold to product antitumor agents, substitution about the rigidifying ring for histamine H4 receptor antagonist synthesis. It is also used as a reactant in the synthesis of CaMKII, VEGFR and FGFR kinase inhibitors and Phosphoinositide-3-kinase, Protein lysine methyltransferase G9a inhibitors.

What is the CAS number for 4-Piperidinol,1-methyl-?

The CAS number of 4-Piperidinol,1-methyl- is 106-52-5.

What is 4-Piperidinol,1-methyl- (106-52-5) used for?

4-Piperidinol,1-methyl-, also known as 4-Hydroxy-1-methylpiperidine, is an organic compound with a clear colorless to yellowish liquid appearance after melting. It is characterized by its unique chemical structure, which makes it a versatile reactant in various synthesis processes.InChI:InChI=1/C6H13NO.ClH/c1-7-4-2-6(8)3-5-7;/h6,8H,2-5H2,1H3;1H

What is the 4-Piperidinol,1-methyl-?

4-Piperidinol,1-methyl- is clear colorless to yellowish liquid after melting, while it's Molecular Formula is C6H13NO. clear colorless to yellowish liquid after melting 4-Hydroxy-1-methylpiperidine is used as reactant for optimization of Novobiocin scaffold to product antitumor agents, substitution about the rigidifying ring for histamine H4 receptor antagonist synthesis. It is also used as a reactant in the synthesis of CaMKII, VEGFR and FGFR kinase inhibitors and Phosphoinositide-3-kinase, Protein lysine methyltransferase G9a inhibitors.

What is the CAS number for 4-Piperidinol,1-methyl-?

The CAS number of 4-Piperidinol,1-methyl- is 106-52-5.

What is 4-Piperidinol,1-methyl- (106-52-5) used for?

4-Piperidinol,1-methyl-, also known as 4-Hydroxy-1-methylpiperidine, is an organic compound with a clear colorless to yellowish liquid appearance after melting. It is characterized by its unique chemical structure, which makes it a versatile reactant in various synthesis processes.InChI:InChI=1/C6H13NO.ClH/c1-7-4-2-6(8)3-5-7;/h6,8H,2-5H2,1H3;1H

Product classification

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106-52-5

Product Name:4-Piperidinol,1-methyl-
Molecular Formula:C₆H₁₃NO
Molecular Weight:115.175
Appearance:clear colorless to yellowish liquid after melting

Inquiry

Product Details

pd_meltingpoint:29-31 °C

Appearance:clear colorless to yellowish liquid after melting

Purity:99%

Buy reliable Quality 4-Piperidinol,1-methyl- 106-52-5 raw material with Honest Price

Molecular Formula:C6H13NO
Molecular Weight:115.175
Appearance/Colour:clear colorless to yellowish liquid after melting
Vapor Pressure:0.00834mmHg at 25°C
Melting Point:29-31 °C
Refractive Index:n20/D 1.479
Boiling Point:200 °C at 760 mmHg
PKA:14.87±0.20(Predicted)
Flash Point:87.8 °C
PSA：23.47000
Density:1.005 g/cm³
LogP:0.01080

4-Piperidinol,1-methyl-(Cas 106-52-5) Usage

Flammability and Explosibility

Notclassified

InChI:InChI=1/C6H13NO.ClH/c1-7-4-2-6(8)3-5-7;/h6,8H,2-5H2,1H3;1H

106-52-5 Relevant articles

Specificities of the enzymes of N-alkyltropane biosynthesis in Brugmansia and Datura

Boswell, Henry D.,Draì?ger, Birgit,McLauchlan, W. Russell,Portsteffen, Andreas,Robins, David J.,Robins, Richard J.,Walton, Nicholas J.

, p. 871 - 878 (1999)

The enzymes N-methylputrescine oxidase (...

Conformation of N-methyl-4-piperidyl 2,4-dinitrobenzoate

Andrau, Laura,White, Jonathan

, p. o60-o61 (2003)

The crystal structure of N-methyl-4-pipe...

Hydrogenation of hindered ketones catalyzed by a silica-supported compact phosphine-Rh system

Kawamorita, Soichiro,Hamasaka, Go,Ohmiya, Hirohisa,Hara, Kenji,Fukuoka, Atsushi,Sawamura, Masaya

, p. 4697 - 4700 (2008)

(Chemical Equation Presented) A heteroge...

Discovery of New Carbonyl Reductases Using Functional Metagenomics and Applications in Biocatalysis

Newgas, Sophie A.,Jeffries, Jack W. E.,Moody, Thomas S.,Ward, John M.,Hailes, Helen C.

, p. 3044 - 3052 (2021)

Enzyme discovery for use in the manufact...

Electrochemical Reductive N-Methylation with CO2Enabled by a Molecular Catalyst

Rooney, Conor L.,Wu, Yueshen,Tao, Zixu,Wang, Hailiang

supporting information, p. 19983 - 19991 (2021/12/01)

The development of benign methylation re...

Synthesis and biological evaluation of new N-substituted 4-(arylmethoxy)piperidines as dopamine transporter inhibitors

Lapa, Gennady B.,Lapa, Alla A.

, p. 203 - 205 (2019/04/25)

The library of new N-substituted 4-(aryl...

Bilobalide B derivative and application of bilobalide B derivative in medicine

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Paragraph 0253; 0254; 0255, (2016/10/09)

The invention relates to a new bilobalid...

106-52-5 Process route

: 1445-73-4
1-Methyl-4-piperidone

: phenylmagnesium bromide

: 71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1
benzene

: 106-52-5
N-methyl-4-hydroxypiperidine

: 4972-68-3
1-methyl-4-phenyl-piperidin-4-ol

: 1,1'-Dimethyl-4-phenyl-decahydro-[3,4']bipyridyl-4,4'-diol

Conditions

Conditions	Yield
anschliessend mit wss. Salzsaeure;

: 3608-67-1
N-methyl-4-piperidyl benzilate

: 106-52-5
N-methyl-4-hydroxypiperidine

: 76-93-7
Benzilic acid

Conditions

Conditions	Yield
With hydrogenchloride; for 100h; Heating; hydrolytic degradation in 0.1 N HCl, H₂O, 0.1 N NaOH/n-propanol (3:1) and without solvens (90 deg C, 50 d), further times;

106-52-5 Upstream products

5382-16-1
4-HYDROXYPIPERIDINE
50-00-0
formaldehyd
695-19-2
N-methyl-4-pyridone
872-50-4
1-methyl-pyrrolidin-2-one

106-52-5 Downstream products

15090-60-5
hydroxy-phenyl-thiazol-2-yl-acetic acid 1-methyl-piperidin-4-yl ester
71579-76-5
(R)-N-methylpiperidin-4-yl 2-cyclohexyl-2-hydroxyphenylacetate
110148-12-4
1-methyl-4-(4-methyl-benzhydryloxy)-piperidine
202646-80-8
FR 194921

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