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1-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDRO-6-QUINOLINYLBORONIC ACID is a boronic acid derivative that plays a significant role in organic synthesis and pharmaceutical research. It features a boronic acid functional group attached to a tetrahydroquinoline scaffold, with a tert-butoxycarbonyl (Boc) protecting group. 1-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDRO-6-QUINOLINYLBORONIC ACID is recognized for its potential in the development of new drugs and bioactive compounds due to the presence of the tetrahydroquinoline moiety, which is found in various biologically active molecules, and the versatility of boronic acids in forming reversible covalent bonds with certain biological targets.

1260150-04-6

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  • (1-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDROQUINOLIN-6-YL)BORONIC ACID

    Cas No: 1260150-04-6

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1260150-04-6 Usage

Uses

Used in Pharmaceutical Research and Development:
1-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDRO-6-QUINOLINYLBORONIC ACID is used as a building block in the synthesis of pharmaceutical drugs and organic molecules. Its unique structure allows for the creation of a wide range of compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDRO-6-QUINOLINYLBORONIC ACID is utilized as a key intermediate for the preparation of various organic compounds. Its boronic acid functional group facilitates the formation of new carbon-carbon bonds, making it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
1-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDRO-6-QUINOLINYLBORONIC ACID is employed as a tool in medicinal chemistry for its ability to form reversible covalent bonds with specific biological targets. This property is crucial in the discovery and optimization of new drug candidates that can modulate biological processes and treat various diseases.
Used in Drug Design:
In the process of drug design, 1-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDRO-6-QUINOLINYLBORONIC ACID is used as a structural element to create novel bioactive compounds. Its incorporation into drug molecules can enhance their binding affinity, selectivity, and overall pharmacological properties, leading to the development of more effective therapeutic agents.
Used in Bioactive Compound Development:
1-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDRO-6-QUINOLINYLBORONIC ACID is utilized in the development of bioactive compounds, which are molecules that can interact with biological systems and produce a therapeutic effect. Its presence in these compounds can contribute to their biological activity and potential use in treating various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1260150-04-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,1,5 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1260150-04:
(9*1)+(8*2)+(7*6)+(6*0)+(5*1)+(4*5)+(3*0)+(2*0)+(1*4)=96
96 % 10 = 6
So 1260150-04-6 is a valid CAS Registry Number.

1260150-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-[(2-methylpropan-2-yl)oxycarbonyl]-3,4-dihydro-2H-quinolin-6-yl]boronic acid

1.2 Other means of identification

Product number -
Other names 1-BOC-1,2,3,4-Tetrahydroquinoline-6-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:1260150-04-6 SDS

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