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179894-36-1

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179894-36-1 Usage

Description

[1-(tert-butoxycarbonyl)-2,2,4-trimethyl-1,2-dihydroquinolin-6-yl]boronic acid is a boronic acid derivative featuring a quinoline core and a tert-butoxycarbonyl protecting group. This chemical compound is utilized in organic synthesis and medicinal chemistry due to its unique structure and functional groups.
Used in Organic Synthesis:
[1-(tert-butoxycarbonyl)-2,2,4-trimethyl-1,2-dihydroquinolin-6-yl]boronic acid is used as a building block in Suzuki-Miyaura cross-coupling reactions for the construction of carbon-carbon bonds. Its boronic acid functionality plays a crucial role in facilitating these reactions, which are vital for creating complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [1-(tert-butoxycarbonyl)-2,2,4-trimethyl-1,2-dihydroquinolin-6-yl]boronic acid is used as a potential candidate in drug discovery and development. The presence of the quinoline core, a common structural motif in many biologically active compounds, makes this compound a promising starting point for the design of new pharmaceutical agents.
Used in Chemical Synthesis:
The tert-butoxycarbonyl protecting group in [1-(tert-butoxycarbonyl)-2,2,4-trimethyl-1,2-dihydroquinolin-6-yl]boronic acid provides stability to the molecule and can be removed under mild conditions. This feature makes the compound a versatile tool in chemical synthesis, allowing for the creation of a variety of related compounds with potential applications in different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 179894-36-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,8,9 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 179894-36:
(8*1)+(7*7)+(6*9)+(5*8)+(4*9)+(3*4)+(2*3)+(1*6)=211
211 % 10 = 1
So 179894-36-1 is a valid CAS Registry Number.

179894-36-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [2,2,4-trimethyl-1-[(2-methylpropan-2-yl)oxycarbonyl]quinolin-6-yl]boronic acid

1.2 Other means of identification

Product number -
Other names I04-1404

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:179894-36-1 SDS

179894-36-1Relevant articles and documents

STEROID RECEPTOR MODULATOR COMPOUNDS AND METHODS

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

Steroid receptor modulator compounds and methods

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

STEROID RECEPTOR MODULATOR COMPOUNDS AND METHODS

-

, (2008/06/13)

Non-steroidal compounds which are high affinity, high selectivity modulators for steroid receptors are disclosed. Also disclosed are pharmaceutical compositions incorporating such compounds, methods for employing the disclosed compounds and compositions for treating patients requiring steroid receptor agonist or antagonist therapy, intermediates useful in the preparation of the compounds and processes for the preparation of the steroid receptor modulator compounds.

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