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5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine is a chemical compound that features a 1,3,2-dioxaborolane moiety attached to an indazol-3-amine structure. This unique arrangement of atoms and functional groups endows the compound with specific reactivity and properties that are valuable in the field of organic synthesis and medicinal chemistry.

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  • 5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-INDAZOL-3-AMINE

    Cas No: 953411-16-0

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  • 953411-16-0 Structure
  • Basic information

    1. Product Name: 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine
    2. Synonyms: 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine;5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-aMi;(3-AMINO-1H-INDAZOL-5-YL)BORONIC ACID PINACOL ESTER
    3. CAS NO:953411-16-0
    4. Molecular Formula: C13H18BN3O2
    5. Molecular Weight: 259
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 953411-16-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 469.9±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.20±0.1 g/cm3 (20 ºC 760 Torr)
    6. Refractive Index: N/A
    7. Storage Temp.: Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
    8. Solubility: N/A
    9. PKA: 14.90±0.40(Predicted)
    10. CAS DataBase Reference: 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine(953411-16-0)
    12. EPA Substance Registry System: 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine(953411-16-0)
  • 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: 953411-16-0(Hazardous Substances Data)

953411-16-0 Usage

Uses

Used in Pharmaceutical Industry:
5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine is used as a synthetic intermediate for the preparation of purineor pyrazolo[3,4-d]pyrimidine-linked isochromene derivatives. These derivatives are of significant interest as they act as phosphoinositide 3-kinase (PI3K) inhibitors.
PI3K inhibitors are a class of compounds that target the PI3K enzyme, which plays a crucial role in cell growth, proliferation, and survival. Overactivity or mutation of the PI3K pathway is implicated in various cancers and other diseases, making PI3K a key target for therapeutic intervention. By inhibiting this enzyme, these isochromene derivatives have the potential to treat cancer and other PI3K-related disorders, thus highlighting the importance of 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine in the development of novel pharmaceutical agents.

Check Digit Verification of cas no

The CAS Registry Mumber 953411-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,3,4,1 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 953411-16:
(8*9)+(7*5)+(6*3)+(5*4)+(4*1)+(3*1)+(2*1)+(1*6)=160
160 % 10 = 0
So 953411-16-0 is a valid CAS Registry Number.

953411-16-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine

1.2 Other means of identification

Product number -
Other names 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine

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:953411-16-0 SDS

953411-16-0Upstream product

953411-16-0Downstream Products

953411-16-0Relevant articles and documents

KINASE INHIBITOR COMPOUNDS AND COMPOSITIONS AND METHODS OF USE

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Paragraph 0175; 0179, (2022/01/04)

Disclosed herein are kinase inhibitor compounds having the structure (I) or a stereoisomer, pharmaceutically acceptable salt, oxide, or solvate thereof, where R1, R2, X, L, Q, and Y are as defined herein. Also disclosed are compositions containing the kinase inhibitor compounds, methods of inhibiting activity of a kinase in a cell, methods of increasing cell proliferation in a population of pancreatic beta cells, methods of treating a subject for a condition associated with insufficient insulin secretion, and methods of treating a subject for a neurological disorder.

ANTIMICROBIAL 4-OXOQUINOLIZINES

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Page/Page column 211; 212, (2012/08/27)

This invention provides novel 4-oxoquinolizine compounds and their uses for a series of broad-spectrum antibiotics having no cross-resistance to existing or emerging classes of antibiotics. In addition the novel 4-oxoquinolizine compounds are useful again

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