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2,2-Spirobi(naphtho(2,3-d)-1,3-dioxole) is a chemical compound characterized by a spirocyclic structure, which consists of two naphthalene rings interconnected by a 1,3-dioxole moiety. This unique arrangement endows the compound with distinctive structural and reactivity features, positioning it as a valuable building block in organic synthesis. Its potential extends to the creation of advanced materials, pharmaceuticals, and agrochemicals, while its intriguing photophysical properties suggest applications in optoelectronics and as a fluorescent probe in biological imaging. 2,2-Spirobi(naphtho(2,3-d)-1,3-dioxole's stability, attributed to its spirocyclic framework, further enhances its utility as a scaffold for designing novel molecules with enhanced properties.

99643-39-7

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99643-39-7 Usage

Uses

Used in Organic Synthesis:
2,2-Spirobi(naphtho(2,3-d)-1,3-dioxole) is utilized as a key building block in organic synthesis due to its distinctive spirocyclic structure and reactivity, facilitating the creation of complex molecules with improved properties.
Used in Advanced Materials Development:
2,2-Spirobi(naphtho(2,3-d)-1,3-dioxole serves as a valuable component in the development of advanced materials, leveraging its unique structure and stability to contribute to the performance and characteristics of new materials.
Used in Pharmaceutical Industry:
2,2-Spirobi(naphtho(2,3-d)-1,3-dioxole) is employed in the pharmaceutical sector, where its potential applications include the design and synthesis of new drugs, taking advantage of its structural features to enhance drug efficacy and properties.
Used in Agrochemicals:
In the agrochemical industry, the compound is used for the development of new agrochemical products, with its unique structure potentially leading to more effective and environmentally friendly solutions.
Used in Optoelectronics:
2,2-Spirobi(naphtho(2,3-d)-1,3-dioxole) is used in optoelectronic devices, capitalizing on its photophysical properties to improve the performance of these devices, such as in solar cells or light-emitting diodes.
Used as a Fluorescent Probe in Biological Imaging:
2,2-Spirobi(naphtho(2,3-d)-1,3-dioxole is applied as a fluorescent probe in biological imaging, where its photophysical properties allow for the visualization and tracking of biological processes at the molecular level.

Check Digit Verification of cas no

The CAS Registry Mumber 99643-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,6,4 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 99643-39:
(7*9)+(6*9)+(5*6)+(4*4)+(3*3)+(2*3)+(1*9)=187
187 % 10 = 7
So 99643-39-7 is a valid CAS Registry Number.

99643-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-spirobi[benzo[f][1,3]benzodioxole]

1.2 Other means of identification

Product number -
Other names 2,2'-Spirobi(naphtho(2,3-d)-1,3-dioxole

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:99643-39-7 SDS

99643-39-7Upstream product

99643-39-7Downstream Products

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