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20394-07-4

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20394-07-4 Usage

Derivative of

Carborane

Class

Boron-containing compounds

Known for

Stability and diverse chemical properties

Contains

Formyl functional group (carbonyl group (C=O) attached to a hydrogen atom)

Potential use

Different sources of media describe the Potential use of 20394-07-4 differently. You can refer to the following data:
1. Building blocks for the synthesis of novel materials
2. Medicinal chemistry for the development of new pharmaceuticals

Unique structure

Makes it an interesting target for further research in the field of boron chemistry and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 20394-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,9 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20394-07:
(7*2)+(6*0)+(5*3)+(4*9)+(3*4)+(2*0)+(1*7)=84
84 % 10 = 4
So 20394-07-4 is a valid CAS Registry Number.

20394-07-4SDS

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 1-formyl-o-carborane

1.2 Other means of identification

Product number -
Other names carbaboranyl aldehyde

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:20394-07-4 SDS

20394-07-4Relevant articles and documents

One-pot synthesis of an indole-substituted 7,8-dicarba-nido-dodecahydroundecaborate(-1)

Neumann,Frank,Hey-Hawkins

supporting information, p. 1748 - 1753 (2015/02/19)

Carbaboranes are increasingly used as pharmacophores to replace phenyl substituents in established drug molecules. In contrast to traditional organic chemistry, elaborate procedures to introduce functionality frequently fail in the case of carbaboranes and their chemistry is often hampered by degradation of the cluster. Herein, the development of a one-pot synthesis of a water-soluble N-nido-dicarbaborato indole is presented, including a proposed mechanism for the reaction sequence. These studies provide useful synthetic tools for the conjugation of two important pharmacophores, indoles and carbaboranes. This journal is

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