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1-Boc-3-methyl-3-hydroxypiperidine, also known as Boc-piperidine, is a versatile chemical compound used as a protecting group for amines in organic synthesis. It is a white solid that is stable under normal conditions and can be easily handled in the laboratory. Boc-piperidine is an important building block in organic chemistry, known for its ability to protect amine groups in various chemical reactions, making it widely used in the pharmaceutical industry for the synthesis of drugs and pharmaceutical intermediates, as well as in the production of agrochemicals, dyes, and other fine chemicals.

1104083-27-3

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1104083-27-3 Usage

Uses

Used in Pharmaceutical Industry:
1-Boc-3-methyl-3-hydroxypiperidine is used as a protecting group for amines in the synthesis of various drugs and pharmaceutical intermediates. Its ability to protect amine groups allows for the efficient and selective synthesis of complex molecules, improving the yield and purity of the final products.
Used in Agrochemical Production:
Boc-piperidine is used as a key intermediate in the production of agrochemicals, where its protecting group properties enable the synthesis of active ingredients with desired properties and improved performance.
Used in Dye Synthesis:
1-Boc-3-methyl-3-hydroxypiperidine is used as a building block in the synthesis of dyes, where its versatility in protecting amine groups allows for the development of dyes with specific color properties and improved stability.
Used in Fine Chemicals Production:
Boc-piperidine is utilized in the production of various fine chemicals, where its protecting group properties contribute to the synthesis of high-quality and specialized chemical products for diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1104083-27-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,4,0,8 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1104083-27:
(9*1)+(8*1)+(7*0)+(6*4)+(5*0)+(4*8)+(3*3)+(2*2)+(1*7)=93
93 % 10 = 3
So 1104083-27-3 is a valid CAS Registry Number.

1104083-27-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl 3-hydroxy-3-methyl-piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 3-hydroxy-3-methylpiperidine-1-carboxylate

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:1104083-27-3 SDS

1104083-27-3Downstream Products

1104083-27-3Relevant academic research and scientific papers

DOPAMINE D2 RECEPTOR LIGANDS

-

Page/Page column 151; 157; 159; 160, (2016/07/05)

The present invention relates to novel dopamine D2 receptor ligands. The invention further relates to functionally-biased dopamine D2 receptor ligands and the use of these compounds for treating or preventing central nervous system and systemic disorders associated with dysregulation of dopaminergic activity. The present invention relates to novel compounds that modulate dopamine D2 receptors. In particular, compounds of the present invention show functional selectivity at the dopamine D2 receptors and exhibit selectivity downstream of the D2 receptors, on the 0- arrestin pathway and/or on the cAMP pathway.

Discovery of (R)-(2-fluoro-4-((-4-methoxyphenyl)ethynyl)phenyl) (3-hydroxypiperidin-1-yl)methanone (ML337), an mGlu3 selective and CNS penetrant negative allosteric modulator (NAM)

Wenthur, Cody J.,Morrison, Ryan,Felts, Andrew S.,Smith, Katrina A.,Engers, Julie L.,Byers, Frank W.,Daniels, J. Scott,Emmitte, Kyle A.,Conn, P. Jeffrey,Lindsley, Craig W.

supporting information, p. 5208 - 5212 (2013/07/26)

A multidimensional, iterative parallel synthesis effort identified a series of highly selective mGlu3 NAMs with submicromolar potency and good CNS penetration. Of these, ML337 resulted (mGlu3 IC50 = 593 nM, mGlu2 IC50 >30 μM) with B:P ratios of 0.92 (mouse) to 0.3 (rat). DMPK profiling and shallow SAR led to the incorporation of deuterium atoms to address a metabolic soft spot, which subsequently lowered both in vitro and in vivo clearance by >50%.

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