Welcome to LookChem.com Sign In|Join Free
  • or
4-METHOXYCARBONYL-1H-INDOLE-2-BORONIC ACID PINACOL ESTER is a chemical compound that serves as a boronic acid ester in organic synthesis and pharmaceutical research. It is known for its versatility in forming carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions and its use as a building block in the synthesis of biologically active molecules, such as pharmaceuticals and agrochemicals. 4-METHOXYCARBONYL-1H-INDOLE-2-BORONIC ACID PINACOL ESTER is valued for its stability and compatibility with a wide range of reaction conditions, making it a crucial tool in organic chemistry research and drug discovery.

1072811-67-6

Post Buying Request

1072811-67-6 Suppliers

Recommended suppliers

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

1072811-67-6 Usage

Uses

Used in Organic Synthesis:
4-METHOXYCARBONYL-1H-INDOLE-2-BORONIC ACID PINACOL ESTER is used as a reagent for forming carbon-carbon bonds in organic synthesis through Suzuki-Miyaura cross-coupling reactions. Its ability to introduce the indole-2-boronic acid pinacol ester unit into various organic molecules makes it a valuable component in the creation of complex organic structures.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-METHOXYCARBONYL-1H-INDOLE-2-BORONIC ACID PINACOL ESTER is used as a building block in the synthesis of biologically active molecules. Its incorporation into the molecular structures of potential drugs allows for the development of new pharmaceuticals with specific therapeutic properties.
Used in Agrochemical Research:
Similarly, in agrochemical research, 4-METHOXYCARBONYL-1H-INDOLE-2-BORONIC ACID PINACOL ESTER is utilized as a building block for the synthesis of biologically active molecules with pesticidal or herbicidal properties. Its application in this field contributes to the development of new and effective agrochemicals for agricultural use.
Used in Research and Development:
4-METHOXYCARBONYL-1H-INDOLE-2-BORONIC ACID PINACOL ESTER is also used as a research tool in academic and industrial laboratories. Its stability and compatibility with a wide range of reaction conditions make it an essential component in the exploration of new chemical reactions and the development of innovative synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 1072811-67-6 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 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1072811-67:
(9*1)+(8*0)+(7*7)+(6*2)+(5*8)+(4*1)+(3*1)+(2*6)+(1*7)=136
136 % 10 = 6
So 1072811-67-6 is a valid CAS Registry Number.

1072811-67-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names -

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:1072811-67-6 SDS

1072811-67-6Upstream product

1072811-67-6Downstream Products

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1072811-67-6