Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1313738-69-0

Post Buying Request

1313738-69-0 Suppliers

Recommended suppliersmore

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

1313738-69-0 Usage

Description

3,5-Difluoro-4-Morpholinophenylboronic Acid Pinacol Ester is a specialized chemical compound that is widely utilized in pharmaceutical and chemical research. As a boronic acid ester, it is instrumental in the Suzuki coupling reaction, a palladium-catalyzed cross-coupling process that facilitates the synthesis of complex organic molecules. Its unique structure, which incorporates both fluorine and morpholine functional groups, renders it highly valuable for the development of novel pharmaceuticals and biologically active compounds. Moreover, the presence of the boronic acid ester enables it to form stable complexes with a variety of compounds, such as sugars and amino acids. It is essential to adhere to proper chemical safety practices when handling and utilizing this compound.

Uses

Used in Pharmaceutical Industry:
3,5-Difluoro-4-Morpholinophenylboronic Acid Pinacol Ester is used as a key intermediate for the synthesis of complex organic molecules, particularly in the development of new pharmaceuticals and biologically active compounds. Its structural features, including fluorine and morpholine functional groups, contribute to its versatility and potential for creating innovative drug candidates.
Used in Chemical Research:
3,5-Difluoro-4-Morpholinophenylboronic Acid Pinacol Ester is used as a reagent in the Suzuki coupling reaction, a palladium-catalyzed cross-coupling process that is essential for the synthesis of complex organic molecules. Its role in this reaction is critical for advancing chemical research and the development of new chemical entities.
Used in the Synthesis of Biologically Active Compounds:
3,5-Difluoro-4-Morpholinophenylboronic Acid Pinacol Ester is used as a building block for the creation of biologically active compounds, thanks to its ability to form stable complexes with various compounds such as sugars and amino acids. This property makes it a valuable tool in the synthesis of molecules with potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1313738-69-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,7,3 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1313738-69:
(9*1)+(8*3)+(7*1)+(6*3)+(5*7)+(4*3)+(3*8)+(2*6)+(1*9)=150
150 % 10 = 0
So 1313738-69-0 is a valid CAS Registry Number.

1313738-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2,6-difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]morpholine

1.2 Other means of identification

Product number -
Other names 3,5-DIFLUORO-4-MORPHOLINOPHENYLBORONIC ACID PINACOL ESTER

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:1313738-69-0 SDS

1313738-69-0Upstream product

1313738-69-0Downstream 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

What can I do for you?
Get Best Price

Get Best Price for 1313738-69-0