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1,2-Benzenediamine, 4,5-bis[(trimethylsilyl)ethynyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

676243-91-7

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676243-91-7 Usage

Chemical structure

A benzene ring with two amino groups (-NH2) at the 1 and 2 positions, and two ethynyl groups (-C≡CH) attached to the 4 and 5 positions, each with a trimethylsilyl (-Si(CH3)3) group.

Molecular weight

Approximately 330.60 g/mol

Appearance

Colorless to pale yellow solid or liquid

Solubility

Soluble in organic solvents such as ethanol, acetone, and dichloromethane

Reactivity

High reactivity due to the presence of amino and ethynyl groups, making it useful as a building block in the synthesis of various organic compounds

Applications

a. Synthesis of polymers, pharmaceuticals, and dyes
b. Catalyst in certain chemical reactions
c. Component in electronic devices due to unique electronic and optical properties

Stability

May be sensitive to air, moisture, and heat, requiring proper storage conditions

Hazards

Potential irritant and harmful if inhaled, ingested, or comes into contact with the skin

Safety precautions

Handle with care, use appropriate personal protective equipment (PPE) such as gloves, goggles, and lab coats, and store in a well-sealed container away from heat and light sources

Regulatory status

May be subject to specific regulations and guidelines depending on the intended use and location, such as the Environmental Protection Agency (EPA) or the European Chemicals Agency (ECHA)

Synonyms

1,2-Phenylenediamine, N-(trimethylsilyl)ethynyl-, 4-((trimethylsilyl)ethynyl)-1,2-phenylenediamine, and other variations

Chemical classification

Aromatic amine and alkynylsilane compound

Functional groups

Amino (-NH2), ethynyl (-C≡CH), and trimethylsilyl (-Si(CH3)3) groups

Synthesis

Typically synthesized through the reaction of a suitable benzene dihalide with trimethylsilylacetylene and subsequent amination using a suitable amine source, such as ammonia or primary amines.

Check Digit Verification of cas no

The CAS Registry Mumber 676243-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,2,4 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 676243-91:
(8*6)+(7*7)+(6*6)+(5*2)+(4*4)+(3*3)+(2*9)+(1*1)=187
187 % 10 = 7
So 676243-91-7 is a valid CAS Registry Number.

676243-91-7SDS

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 4,5-bis(2-trimethylsilylethynyl)benzene-1,2-diamine

1.2 Other means of identification

Product number -
Other names -

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:676243-91-7 SDS

676243-91-7Downstream Products

676243-91-7Relevant academic research and scientific papers

Synthesis and Bergman cyclization of a β-extended porphyrenediyne

Spence, John D.,Cline, Eric D.,Llagostera, Domingo M.,O'Toole, Patrick S.

, p. 180 - 181 (2004)

Condensation of a porphyrin-2,3-dione with a 1,2-diaminoarenediyne affords a β-extended porphyrinic-enediyne: upon thermal Bergman cyclization the quinoxaline spacer positioned between the macrocycle and the enediyne prevents tandem radical cyclization to

Syntheses, thermal reactivities, and computational studies of aryl-fused quinoxalenediynes: Effect of extended benzannelation on Bergman cyclization energetics

Spence, John D.,Rios, Andro C.,Frost, Megan A.,McCutcheon, Claire M.,Cox, Christopher D.,Chavez, Sonia,Fernandez, Ramiro,Gherman, Benjamin F.

, p. 10329 - 10339 (2012)

A series of [b]-fused 6,7-diethynylquinoxaline derivatives have been synthesized through an imine condensation strategy to examine the effect of extended benzannelation on the thermal reactivity of enediynes. Absorption and emission spectra of the highly

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