Welcome to LookChem.com Sign In|Join Free

CAS

  • or
N,N-Dimethyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethanamine is a borate ester derivative with the molecular formula C16H27BO3N. It is a clear, colorless liquid at room temperature and is soluble in both water and organic solvents. This chemical is known for its ability to form stable complexes with other organic compounds, making it a versatile reagent in various chemical reactions.

873078-93-4

Post Buying Request

873078-93-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • dimethyl({2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethyl})amine

    Cas No: 873078-93-4

  • USD $ 1.9-2.9 / Gram

  • 100 Gram

  • 1000 Metric Ton/Month

  • Chemlyte Solutions
  • Contact Supplier

873078-93-4 Usage

Uses

Used in Organic Synthesis:
N,N-Dimethyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethanamine is used as a reagent in organic synthesis for its ability to form stable complexes with other organic compounds, facilitating various chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N,N-Dimethyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethanamine is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its reactivity and ability to form stable complexes.
Used in Agrochemical Industry:
N,N-Dimethyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethanamine is also utilized in the agrochemical industry for the synthesis of agrochemicals, where its reactivity and complex-forming ability contribute to the development of effective products.
Used as a Cross-linking Agent in Polymer Production:
In the polymer industry, N,N-Dimethyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethanamine is used as a cross-linking agent, enhancing the properties of polymers by forming stable connections between polymer chains.
Used as a Stabilizer in Coatings and Adhesives Formulation:
N,N-Dimethyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethanamine serves as a stabilizer in the formulation of coatings and adhesives, improving their performance and durability by forming stable complexes with other components in the formulation.

Check Digit Verification of cas no

The CAS Registry Mumber 873078-93-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,0,7 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 873078-93:
(8*8)+(7*7)+(6*3)+(5*0)+(4*7)+(3*8)+(2*9)+(1*3)=204
204 % 10 = 4
So 873078-93-4 is a valid CAS Registry Number.

873078-93-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-Dimethyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethanamine

1.2 Other means of identification

Product number -
Other names N,N-dimethyl-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethanamine

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:873078-93-4 SDS

873078-93-4Relevant articles and documents

PYRROLO [2, 3-B] PYRIDINES OR PYRROLO [2, 3-B] PYRAZINES AS HPK1 INHIBITOR AND THE USE THEREOF

-

Paragraph 0401; 0874-0876, (2020/01/08)

Disclosed herein is a compound of Formula (AIII) or (III), or a stereoisomer thereof, or a pharmaceutically acceptable salt thereof, and pharmaceutical compositions comprising thereof. Also disclosed is a method of treating HPK1 related disorders or diseases by using the compound disclosed herein.

MAP4K4 INHIBITORS

-

Paragraph 00206, (2019/05/02)

This invention relates to pyrrolopyrimidine comprising compounds that may be useful as inhibitors of Mitogen-activated Protein Kinase Kinase Kinase Kinase-4 (MAP4K4). The invention also relates to the use of these pyrrolopyrimidine comprising compounds, f

PYRAZOLOPYRIMIDIN-2-YL DERIVATIVES AS JAK INHIBITORS

-

Page/Page column 91; 92, (2015/06/25)

New pyrazolopyridmiin-2-yl derivatives are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Janus Kinases (JAK).

SUBSTITUTED PYRIDOPYRAZINES AS NOVEL SYK INHIBITORS

-

Paragraph 0156; 0157, (2014/05/08)

Provided are pyridopyrazine compounds of formula (1), pharmaceutical compositions thereof and methods of use therefore, wherein R1, R2, R3, R4 and m are as defined in the specification.

SUBSTITUTED PYRIDOPYRAZINES AS NOVEL SYK INHIBITORS

-

Page/Page column 34, (2013/02/27)

Provided are certain pyridopyrazine compounds, pharmaceutical compositions thereof and methods of use therefor.

AZACARBOLINE DERIVATIVES, PREPARATION METHOD THEREOF AND THERAPEUTIC USE OF SAME

-

Page/Page column 69, (2011/08/04)

The invention relates to novel azacarbonlines having formula (I), wherein: R3, R4 represent independently H; hal; CF3; substituted oxy, optionally substituted alkoxy; optionally substituted amino; substituted carbonyl; optionally substituted carboxyl; optionally substituted amide; sulphur, such as optionally substituted sulphones, sulphoxides or sulphides; linear, branched or cyclic C1-C10 alkyl optionally comprising an optionally substituted heteroatom; optionally substituted linear, branched or cyclic C2-C7 alkenyl; optionally substituted linear or branched C2-C6 alkynyl; optionally substituted aryl or heteroaryl; of which may be optionally substituted; in the form of a base or an acid addition salt. The invention also relates to the use of same in therapeutics for the treatment of cancer and to synthesis methods.

KINASE INHIBITORS AND METHOD OF TREATING CANCER WITH SAME

-

Page/Page column 187-188, (2010/11/03)

The invention is directed to a compound represented by the following structural formula and pharmaceutically acceptable salts thereof: Compounds represented by this structural formula are kinase inhibitors and are therefore disclosed herein for the treatment of cancer. Definitions for the variables in the structural formula are provided herein.

PYRROLO[2,3-d]PYRIMIDINES THAT MODULATE ACK1 AND LCK ACTIVITY

-

Page/Page column 46-47, (2010/02/15)

Compounds that modulate the action of ACK1 and LCK, and related compositions methods for treating ACK1- and LCK-mediated diseases are described. In one aspect, the compounds have the general structure: where the values of the substituents are provided her

Furanopyridine derivatives and methods of use

-

Page/Page column 42; 48, (2010/10/20)

The present invention relates to furanopyridine compounds having the general Formula I: and stereoisomers, tautomers, solvates, pharmaceutically acceptable salts and derivatives, and prodrugs thereof. The invention also includes pharmaceutical composition

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 873078-93-4