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3-ethyl-2-[2-[(3-ethyl-3H-benzothiazol-2-ylidene)methyl]but-1-enyl]benzothiazolium iodide is a complex organic compound with the molecular formula C21H20IN3S2. It is a benzothiazolium salt, characterized by the presence of two benzothiazole rings, one of which is substituted with an ethyl group. The compound features a butenyl side chain that connects the two benzothiazole rings, with one end of the side chain bearing a methyl group that is part of a ylidene group. This ylidene group is a key structural feature, contributing to the compound's reactivity and properties. The iodide counterion is associated with the positively charged benzothiazolium cation, forming an ionic bond. 3-ethyl-2-[2-[(3-ethyl-3H-benzothiazol-2-ylidene)methyl]but-1-enyl]benzothiazolium iodide is likely to be used in various chemical applications, such as in the synthesis of dyes, pigments, or as a reagent in organic reactions, due to its unique structure and potential electronic properties.

909-63-7

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909-63-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 909-63-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,0 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 909-63:
(5*9)+(4*0)+(3*9)+(2*6)+(1*3)=87
87 % 10 = 7
So 909-63-7 is a valid CAS Registry Number.
InChI:InChI=1/C23H25N2S2.HI/c1-4-17(15-22-24(5-2)18-11-7-9-13-20(18)26-22)16-23-25(6-3)19-12-8-10-14-21(19)27-23;/h7-16H,4-6H2,1-3H3;1H/q+1;/p-1

909-63-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-2-[2-[(3-ethyl-1,3-benzothiazol-3-ium-2-yl)methylidene]butylidene]-1,3-benzothiazole,iodide

1.2 Other means of identification

Product number -
Other names 3-ethyl-2-[2-(3-ethyl-3H-benzothiazol-2-ylidenemethyl)-but-1-enyl]-benzothiazolium,iodide

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

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More Details:909-63-7 SDS

909-63-7Relevant academic research and scientific papers

CONDENSATION OF VILSMEIER COMPLEXES WITH HETEROCYCLIC COMPOUNDS. SYNTHESIS OF CARBOCYANINES

Makin, S. M.,Pomogaev, A. I.

, p. 1916 - 1918 (2007/10/02)

Carbocyanine dyes are formed in the reaction of the quaternary salts of heterocyclic bases containing an active methyl group with the complexes of carboxamides and phosphorus oxychloride.A series of carbocyanines were synthesized, including those containing various substituents at the meso position of the trimethine chain.

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