1063-92-9

Basic information

• Product Name: 1-methyl-2-[3-(1-methylnaphtho[1,2-d]thiazol-2(1H)-ylidene)-2-phenyl-1-propenyl]naphtho[1,2-d]thiazolium chloride
• Synonyms: Naphtho(1,2-d)thiazolium, 1-methyl-2-(3-(1-methylnaphtho(1,2-d)thiazol-2(1H)-ylidene)-2-phenyl-1-propen-1-yl)-, chloride (1:1); 1-Methyl-2-(3-(1-methylnaphtho(1,2-d)thiazol-2(1H)-ylidene)-2-phenyl-1-propenyl)naphtho(1,2-d)thiazolium chloride; Naphtho(1,2-d)thiazolium, 1-methyl-2-(3-(1-methylnaphtho(1,2-d)thiazol-2(1H)-ylidene)-2-phenyl-1-propenyl)-, chloride; 1-methyl-2-[(1E,3Z)-3-(1-methylnaphtho[1,2-d][1,3]thiazol-2(1H)-ylidene)-2-phenylprop-1-en-1-yl]naphtho[1,2-d][1,3]thiazol-1-ium chloride
• CAS NO: 1063-92-9
• Molecular Formula: C₃₃H₂₅ClN₂S₂
• Molecular Weight: 549.148
• EINECS: 213-901-0
• Mol File: 1063-92-9.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: 1-methyl-2-[3-(1-methylnaphtho[1,2-d]thiazol-2(1H)-ylidene)-2-phenyl-1-propenyl]naphtho[1,2-d]thiazolium chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-2-[3-(1-methylnaphtho[1,2-d]thiazol-2(1H)-ylidene)-2-phenyl-1-propenyl]naphtho[1,2-d]thiazolium chloride(1063-92-9)
• EPA Substance Registry System: 1-methyl-2-[3-(1-methylnaphtho[1,2-d]thiazol-2(1H)-ylidene)-2-phenyl-1-propenyl]naphtho[1,2-d]thiazolium chloride(1063-92-9)

Safety Data

• Hazardous Substances Data: 1063-92-9(Hazardous Substances Data)

Usage

Chemical class

Thiazolium salt

Explanation

Different sources of media describe the Explanation of 1063-92-9 differently. You can refer to the following data:
1. It is a compound containing a thiazolium ring, specifically a 1-methyl-2-naphtho[1,2-d]thiazol-2(1H)-ylidene group.
2. The compound consists of two main functional groups, which contribute to its chemical properties and reactivity.
3. The compound is commonly used as a catalyst in organic synthesis, promoting and accelerating chemical reactions.
4. The compound's properties make it suitable for use as a fluorescent marker, aiding in the visualization and analysis of biological processes and medical imaging.
5. The chloride form of the compound is often used due to its increased stability and reactivity, making it more suitable for various applications.
6. The compound's unique properties and applications make it an important and valuable tool in the fields of chemistry, biology, and medicine.

Functional groups

2-naphtho[1,2-d]thiazol-2(1H)-ylidene and 2-phenyl-1-propenyl

Usage in scientific research

Catalyst in organic synthesis

Usage in industrial applications

Fluorescent marker in biological and medical imaging studies

Chloride form

Stability and reactivity in chemical reactions

Importance in various fields

Valuable tool in chemical research and development