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(3-([(TERT-BUTOXYCARBONYL)AMINO]METHYL)PYRIDIN-4-YL)BORONIC ACID is a complex organic compound belonging to the class of boronic acids, characterized by a pyridine ring attached to a boronic acid group and an amino methyl group with a tert-butoxycarbonyl (BOC) protective group. (3-([(TERT-BUTOXYCARBONYL)AMINO]METHYL)PYRIDIN-4-YL)BORONIC ACID is known for its role as an important reagent in organic chemistry, with its properties and behavior significantly influenced by the presence of the boronic acid and BOC-protected amino groups.

433969-29-0

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433969-29-0 Usage

Uses

Used in Organic Synthesis:
(3-([(TERT-BUTOXYCARBONYL)AMINO]METHYL)PYRIDIN-4-YL)BORONIC ACID is used as a reagent in organic synthesis for its ability to contribute to the formation of pharmaceuticals or other complex organic compounds. Its unique structure and functional groups make it a valuable component in the synthesis of various organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (3-([(TERT-BUTOXYCARBONYL)AMINO]METHYL)PYRIDIN-4-YL)BORONIC ACID is used as a building block for the development of new drugs. Its presence of the boronic acid group and BOC-protected amino groups allows for versatile chemical reactions and modifications, enabling the creation of novel pharmaceutical compounds with potential therapeutic applications.
Used in Chemical Research:
(3-([(TERT-BUTOXYCARBONYL)AMINO]METHYL)PYRIDIN-4-YL)BORONIC ACID is also utilized in chemical research as a model compound to study the properties and reactivity of boronic acids and their derivatives. Its unique structure provides insights into the behavior of similar compounds and contributes to the advancement of organic chemistry knowledge.

Check Digit Verification of cas no

The CAS Registry Mumber 433969-29-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,3,9,6 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 433969-29:
(8*4)+(7*3)+(6*3)+(5*9)+(4*6)+(3*9)+(2*2)+(1*9)=180
180 % 10 = 0
So 433969-29-0 is a valid CAS Registry Number.

433969-29-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-[[(2-methylpropan-2-yl)oxycarbonylamino]methyl]pyridin-4-yl]boronic acid

1.2 Other means of identification

Product number -
Other names 3-(tert-butoxycarbonylaminomethyl)pyridyl-4-boronic acid

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:433969-29-0 SDS

433969-29-0Upstream product

433969-29-0Relevant academic research and scientific papers

Identification, synthesis, and activity of novel blockers of the voltage-gated potassium channel Kv1.5

Peukert, Stefan,Brendel, Joachim,Pirard, Bernard,Brüggemann, Andrea,Below, Peter,Kleemann, Heinz-Werner,Hemmerle, Horst,Schmidt, Wolfgang

, p. 486 - 498 (2003)

The voltage-gated potassium channel Kv1.5 is regarded as a promising target for the development of new atrial selective drugs with fewer side effects. In the present study the discovery of ortho, ortho-disubstituted bisaryl compounds as blockers of the Kv

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