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191529-09-6

191529-09-6

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191529-09-6 Usage

General Description

2,4,6-tribromobenzene-1,3,5-tricarbaldehyde is a chemical compound with a molecular formula C9H3Br3O3. It is a symmetrical molecule with three aldehyde groups attached to a benzene ring, each at the 1, 3, and 5 positions. The compound contains three bromine atoms at the 2, 4, and 6 positions on the benzene ring. This chemical is primarily used in organic synthesis and as a building block for more complex molecules. It is also used in the production of coordination complexes and as a reagent in chemical reactions. Furthermore, this compound has potential applications in materials science and as a reagent for environmental analysis.

Check Digit Verification of cas no

The CAS Registry Mumber 191529-09-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,5,2 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 191529-09:
(8*1)+(7*9)+(6*1)+(5*5)+(4*2)+(3*9)+(2*0)+(1*9)=146
146 % 10 = 6
So 191529-09-6 is a valid CAS Registry Number.

191529-09-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tribromobenzene-1,3,5-tricarbaldehyde

1.2 Other means of identification

Product number -
Other names 2,4,6-tribromobenzene-1,3,5-tricarboxaldehyde

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:191529-09-6 SDS

191529-09-6Relevant articles and documents

Interfacial synthesis of crystalline two-dimensional cyano-graphdiyne

Chen, Siqi,Li, Zhibo,Pan, Qingyan,Shao, Feng,Sun, Qingzhu,Wu, Chenyu,Zhang, Zhaohui,Zhao, Yingjie

supporting information, p. 3210 - 3213 (2020/03/23)

A well-defined crystalline cyano-functionalized graphdiyne (CN-GDY) is synthesized at a liquid/liquid interface through alkyne-alkyne coupling reactions. The configurations and nanostructures of CN-GDY were well characterized by TEM, SEM, AFM, XPS, and Raman spectroscopy. HR-TEM and selected area electron diffraction (SAED) in combination with structure simulation firmly revealed a 9-fold stacking mode for CN-GDY.

An efficient route to 1,3,5-triazido-2,4,6-tricyanobenzene

Becke, Martin,Voss, Karsten,Villinger, Alexander,Schulz, Axel

, p. 643 - 649,7 (2020/08/31)

An efficient synthetic route starting from 1,3,5-trimethylbenzene is described for binary 1,3,5- triazido-2,4,6-tricyanobenzene. Besides 1,3,5-triazido-2,4,6-tricyanobenzene, all intermediates have been isolated and fully characterized.

En route to archimedene: Total synthesis of C3h-symmetric [7]phenylene

Bruns, Dirk,Miura, Hirokazu,Vollhardt, K. Peter C.,Stanger, Amnon

, p. 549 - 552 (2007/10/03)

(Matrix presented) The total synthesis of C3h-symmetric [7]phenylene has been accomplished by triple cobalt-catalyzed cycloisomerization of an appropriate nonayne. Its spectral data are in accord with the expectations for a triply angularly fus

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