Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1072812-69-1

Post Buying Request

1072812-69-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1072812-69-1 Usage

Description

7-Methoxy-1H-Indole-2-Boronic Acid Pinacol Ester is a chemical compound that belongs to the class of organic compounds known as indoles. It is characterized by an indole group, which is a bicyclic entity consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. In this compound, the indole group is substituted by a methoxy group at the 7th position and a boronic acid pinacol ester group at the 2nd position. Boronic acid esters are known for their importance in Suzuki coupling reactions, which are commonly used in organic synthesis. The unique features of this compound suggest that it may be valuable in chemical synthesis and potentially in the development of pharmaceuticals or other chemical products.

Uses

Used in Chemical Synthesis:
7-Methoxy-1H-Indole-2-Boronic Acid Pinacol Ester is used as a key intermediate in chemical synthesis for its ability to participate in Suzuki coupling reactions. This allows for the formation of carbon-carbon bonds, which are crucial in the synthesis of complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 7-Methoxy-1H-Indole-2-Boronic Acid Pinacol Ester is used as a building block for the development of new drugs. Its unique structure and reactivity in Suzuki coupling reactions make it a valuable component in the design and synthesis of novel pharmaceutical compounds with potential therapeutic applications.
Used in Material Science:
7-Methoxy-1H-Indole-2-Boronic Acid Pinacol Ester can also be utilized in material science for the synthesis of advanced materials with specific properties. Its ability to form carbon-carbon bonds through Suzuki coupling reactions can contribute to the development of new materials with tailored characteristics for various applications, such as electronics, sensors, or energy storage.

Check Digit Verification of cas no

The CAS Registry Mumber 1072812-69-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,2,8,1 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1072812-69:
(9*1)+(8*0)+(7*7)+(6*2)+(5*8)+(4*1)+(3*2)+(2*6)+(1*9)=141
141 % 10 = 1
So 1072812-69-1 is a valid CAS Registry Number.

1072812-69-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

1.2 Other means of identification

Product number -
Other names 7-methoxy-2-(4,4,5,5-tetramethyl[1,3,2]-dioxaborolan-2-yl)-1H-indole

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:1072812-69-1 SDS

1072812-69-1Upstream product

1072812-69-1Downstream Products

1072812-69-1Relevant articles and documents

INHIBITORS OF CAMKK2 AND USES OF SAME

-

Paragraph 0102; 0103; 0118; 0119, (2020/12/08)

The present disclosure provides compounds suitable for inhibiting CaMKK2. Also provided are compositions and methods of treating diseases associated with CaMKK2.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1072812-69-1