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2-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 3-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2,4-diaza-3-boratricyclo[7.3.1.0 ,13]trideca-1(13),5,7,9,11-pentaene

    Cas No: 950511-17-8

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  • 2-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine

    Cas No: 950511-17-8

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  • 2-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine

    Cas No: 950511-17-8

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  • 950511-17-8 Structure
  • Basic information

    1. Product Name: 2-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine
    2. Synonyms: 2-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine;3-[3-(Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2,4-diaza-3-boratricyclo[7.3.1.0^{5,13}]trid;3-[3-(Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2,4-diaza-3-boratricyclo[7.3.1.0^{5,13}]trideca- 1(13),5,7,9,11-pentaene;(3-(1H-NAPHTHO[1,8-DE][1,3,2]DIAZABORININ-2(3H)-YL)PHENYL)BORONIC ACID PINACOL ESTER;m-Benzenediboronic Acid Pinacol Ester, 1,8-Diaminonaphthalene, Protected
    3. CAS NO:950511-17-8
    4. Molecular Formula: C22H24B2N2O2
    5. Molecular Weight: 370.07
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 950511-17-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine(950511-17-8)
    11. EPA Substance Registry System: 2-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine(950511-17-8)
  • 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: 950511-17-8(Hazardous Substances Data)

950511-17-8 Usage

Chemical class

Boron-containing compounds

Core structure

Naphtho[1,8-de][1,3,2]diazaborinine

Ring system

2,3-dihydro-1H-naphtho

Substituent

2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]

Potential applications

Materials science, organic synthesis, and chemical research

Unique structure

Interesting target for further study and exploration

Relevance

Various fields of chemistry and related disciplines

Check Digit Verification of cas no

The CAS Registry Mumber 950511-17-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,0,5,1 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 950511-17:
(8*9)+(7*5)+(6*0)+(5*5)+(4*1)+(3*1)+(2*1)+(1*7)=148
148 % 10 = 8
So 950511-17-8 is a valid CAS Registry Number.

950511-17-8SDS

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 2-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2,3-dih ydro-1H-naphtho[1,8-de][1,3,2]diazaborinine

1.2 Other means of identification

Product number -
Other names 1-o-Methoxycarbonylphenyl-3-m-nitrophenyltriazen

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:950511-17-8 SDS

950511-17-8Relevant articles and documents

Direct transformation from arylamines to aryl naphthalene-1,8-diamino boronamides: A metal-free sandmeyer-type process

Ding, Siyi,Ma, Qiang,Zhu, Min,Ren, Huaping,Tian, Shaopeng,Zhao, Yuzhen,Miao, Zongcheng

, (2019/02/07)

A direct metal-free transformation from arylamines to aryl naphthalene-1,8-diamino boronamides, a type of masked boronic acid, has been developed based on Sandmeyer-type reactions. A nonsymmetrical diboron reagent, B(pin)-B(dan), was utilized as the boryl

IMIDAZOPYRIDAZINE DERIVATIVES AS MODULATORS OF THE GABAA RECEPTOR ACTIVITY.

-

, (2016/01/01)

The present invention relates to imidazopyridazine derivatives. More particularly, it relates to 4-(biphenyl-3-yl)-7H-imidazo[4,5-c]pyridazine derivatives of formula (I) and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R and R6 are as defined in the description. The imidazopyridazine derivatives of the present invention modulate the activity of the GABAA receptor. They are useful in the treatment of a number of conditions, including pain.

Chemical Compounds

-

, (2014/06/25)

The present invention relates to imidazopyridazine derivatives. More particularly, it relates to 4-(biphenyl-3-yl)-7H-imidazo[4,5-c]pyridazine derivatives of formula (I): and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4 and R5 are as defined in the description. The imidazopyridazine derivatives of the present invention modulate the activity of the GABAA receptor. They are useful in the treatment of a number of conditions, including pain.

Differentially protected benzenediboronic acids: Divalent cross-coupling modules for the efficient synthesis of boron-substituted oligoarenes

Noguchi, Hiroyoshi,Shioda, Takayuki,Chou, Chih-Ming,Suginome, Michinori

, p. 377 - 380 (2008/09/19)

On the basis of the boron-masking strategy, new divalent cross-coupling modules have been designed for the efficient synthesis of boronsubstituted oligoarenes. The modules, i.e., monoprotected o-, m-, and p-benzenediboronic acid derivatives, undergo highly selective SuzukiMiyaura coupling with sp 2 iodides, bromides, chlorides, and triflates, affording coupling products in which the protected boronyl groups are left intact.

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