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189889-45-0

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189889-45-0 Usage

Chemical class

Belongs to the class of piperidines, which are heterocyclic compounds with a six-membered ring containing one nitrogen atom.

Synonyms

Also known as N-Boc-4-ethoxycarbonylmethoxypiperidine.

Use

Used as an intermediate in the synthesis of pharmaceuticals and bioactive compounds.

Structural features

Characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group and an ethoxycarbonylmethoxy group attached to the piperidine ring.

Boc group function

Serves as a protective agent during chemical reactions, allowing for selective modification of the piperidine molecule.

Ethoxycarbonylmethoxy group

This group is attached to the 4-position of the piperidine ring, providing additional functionalization and reactivity.

Organic synthesis

1-Boc-4-ethoxycarbonylmethoxypiperidine is a valuable building block in organic synthesis.

Applications

Has potential applications in drug discovery and medicinal chemistry due to its unique structure and reactivity.

Solubility

The solubility of this compound may vary depending on the solvent used, but it is generally soluble in common organic solvents like methanol, ethanol, and dimethyl sulfoxide (DMSO).

Stability

The compound is generally stable under normal laboratory conditions, but it should be stored away from light, heat, and moisture to maintain its integrity.

Check Digit Verification of cas no

The CAS Registry Mumber 189889-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,8,8 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 189889-45:
(8*1)+(7*8)+(6*9)+(5*8)+(4*8)+(3*9)+(2*4)+(1*5)=230
230 % 10 = 0
So 189889-45-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H25NO5/c1-5-18-12(16)10-19-11-6-8-15(9-7-11)13(17)20-14(2,3)4/h11H,5-10H2,1-4H3

189889-45-0SDS

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 tert-butyl 4-(2-ethoxy-2-oxoethoxy)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names F2158-1141

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:189889-45-0 SDS

189889-45-0Relevant articles and documents

IRAK DEGRADERS AND USES THEREOF

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Paragraph 00618-00619, (2021/08/13)

The present invention provides compounds, compositions thereof, and methods of using the same.

IRAK DEGRADERS AND USES THEREOF

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Paragraph 00920; 002524-002526, (2021/01/23)

The present invention provides compounds, compositions thereof, and methods of using the same. The compounds include an IRAK binding moiety capable of binding to IRAK4 and a degradation inducing moiety (DIM). The DIM could be DTM a ligase binding moiety (LBM) or lysine mimetic. The compounds could be useful as IRAK protein kinase inhibitors and applied to IRAK mediated disorders.

IRAK DEGRADERS AND USES THEREOF

-

Paragraph 00794; 001022-001024, (2021/01/23)

The present invention provides compounds, compositions thereof, and methods of using the same. The compounds include an IRAK binding moiety and a degradation inducing moiety (DIM). The DIM could be DTM a ligase binding moiety (LBM) or lysine mimetic. The compounds could be useful as IRAK protein kinase inhibitors and applied to IRAK mediated disorders.

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