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DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE is a complex organic compound characterized by its unique structure that includes carbon, hydrogen, nitrogen, and boron elements. It is a tertiary amine with a dimethyl substituent, a dioxaborolane moiety, and a benzyl group. The presence of the dioxaborolane group suggests its potential utility in cross-coupling reactions, a common technique in organic synthesis. DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE's specific structure and functionality could make it suitable for various applications in pharmaceuticals, materials science, and other chemical industries, with further research likely to uncover additional uses and properties.

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  • dimethyl({[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl})amine

    Cas No: 909391-56-6

  • USD $ 1.9-2.9 / Gram

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  • 909391-56-6 Structure
  • Basic information

    1. Product Name: DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE
    2. Synonyms: DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE;3-(N,N-Dimethylaminomethyl)phenylboronic acid, pinacol ester;3-Dimethylaminomethylphenylboronic acid pinacol ester;Dimethyl[[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]amine;N,N-diMethyl-1-(3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl)MethanaMine;3-Dimethylaminomethylphenylboronic acid pinacol ester Dimethyl[[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]amine;N,N-dimethyl(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanamine;N,N-Dimethyl-1-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methylamine
    3. CAS NO:909391-56-6
    4. Molecular Formula: C15H24BNO2
    5. Molecular Weight: 261.18
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 909391-56-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 340.8±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.00
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. PKA: 8.78±0.28(Predicted)
    10. CAS DataBase Reference: DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE(909391-56-6)
    12. EPA Substance Registry System: DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE(909391-56-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 909391-56-6(Hazardous Substances Data)

909391-56-6 Usage

Uses

Used in Organic Synthesis:
DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE is used as a synthetic intermediate for the preparation of various organic compounds due to its dioxaborolane moiety, which is commonly utilized in cross-coupling reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE is used as a building block for the development of new drugs, leveraging its unique chemical structure to create molecules with specific therapeutic properties.
Used in Materials Science:
DIMETHYL-[3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-BENZYL]-AMINE is used as a component in the synthesis of advanced materials, potentially contributing to the development of new polymers, coatings, or other materials with specialized properties.

Check Digit Verification of cas no

The CAS Registry Mumber 909391-56-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,3,9 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 909391-56:
(8*9)+(7*0)+(6*9)+(5*3)+(4*9)+(3*1)+(2*5)+(1*6)=196
196 % 10 = 6
So 909391-56-6 is a valid CAS Registry Number.

909391-56-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-1-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine

1.2 Other means of identification

Product number -
Other names 3-[(N,N-dimethylamino)methyl]phenylboronic 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:909391-56-6 SDS

909391-56-6Downstream Products

909391-56-6Relevant articles and documents

Iron-catalyzed C-H borylation of arenes

Dombray, Thomas,Werncke, C. Gunnar,Jiang, Shi,Grellier, Mary,Vendier, Laure,Bontemps, Sébastien,Sortais, Jean-Baptiste,Sabo-Etienne, Sylviane,Darcel, Christophe

supporting information, p. 4062 - 4065 (2015/04/14)

Well-defined iron bis(diphosphine) complexes are active catalysts for the dehydrogenative C-H borylation of aromatic and heteroaromatic derivatives with pinacolborane. The corresponding borylated compounds were isolated in moderate to good yields (25-73%) with a 5 mol% catalyst loading under UV irradiation (350 nm) at room temperature. Stoichiometric reactivity studies and isolation of an original trans-hydrido(boryl)iron complex, Fe(H)(Bpin)(dmpe)2, allowed us to propose a mechanism showing the role of some key catalytic species.

2- (4-0X0-4H-QUINAZ0LIN-3-YL) ACETAMIDES AND THEIR USE AS VASOPRESSIN V3 ANTAGONISTS

-

Page/Page column 43-44, (2010/11/23)

The present invention relates to 2-(4-oxo4H-quinazolin-3-yl)acetamicle derivatives of formula (I), and to their use as vasopressin V3 antagonists, particularly for the treatment of depression.

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