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24040-37-7 Usage

Chemical structure

1-(9H-fluoren-9-yl)triaza-1,2-dien-2-ium is a chemical compound with a molecular structure containing a fluorenyl group attached to a triaza-dien-ium moiety.

Potential applications

It has potential applications in various fields such as organic synthesis and materials science due to its unique structural features and chemical properties.

Building block

It can be used as a building block for the synthesis of complex organic molecules.


It can be used as a precursor for the preparation of functional materials.

Triaza-dien-ium component

Its triaza-dien-ium component could impart unique electronic and optical properties.

Electronic and photonic devices

It is potentially useful in the development of new materials for electronic and photonic devices.

Further research

Further research and exploration of its properties and potential applications may lead to the development of novel technologies and products.

Check Digit Verification of cas no

The CAS Registry Mumber 24040-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,4 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24040-37:
67 % 10 = 7
So 24040-37-7 is a valid CAS Registry Number.



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


1.1 GHS Product identifier

Product name 9-azido-9H-fluorene

1.2 Other means of identification

Product number -
Other names 9-Azidofluoren

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:24040-37-7 SDS

24040-37-7Relevant articles and documents



, p. 2027,2028 (1954)


Optimal Destabilization of DNA Double Strands by Single-Nucleobase Caging

Seyfried, Patrick,Heinz, Marcel,Pintér, Gy?rgy,Kl?tzner, Dean-Paulos,Becker, Yvonne,Bolte, Michael,Jonker, Hendrik R. A.,Stelzl, Lukas S.,Hummer, Gerhard,Schwalbe, Harald,Heckel, Alexander

supporting information, p. 17568 - 17576 (2018/11/10)

Photolabile protecting groups are widely used to trigger oligonucleotide activity. The ON/OFF-amplitude is a critical parameter. An experimental setup has been developed to identify protecting group derivatives with superior caging properties. Bulky rests



Paragraph 0095-0097, (2016/04/20)

Methods and reagents for enhancing cellular uptake of a cargo molecule by covalently bonding optionally-substituted fluorenyl groups to the cargo molecules, where cellular uptake includes at least partial uptake into the cytosol. Useful fluorenylation reagents include those of formula: and salts thereof where variables are as defined. Cargo molecules include peptides and proteins. Also provided are fluorenylated cargo molecules, including fluorenylated peptides and proteins.

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