- CAS 34263-37-1
- Purity 99%
3-allyl-2-[3-[3-allylbenzothiazol-2(3H)-ylidene]prop-1-enyl]benzothiazolium iodide
High quality purity >99% 3-allyl-2-[3-[3-allylbenzothiazol-2(3H)-ylidene]prop-1-enyl]benzothiazolium iodide 34263-37-1 for sale We supply high quality 3-allyl-2-[3-[3-allylbenzothiazol-2(3H)-ylidene]prop-1-enyl]benzothiazolium iodide (CAS 34263-37-1), in stock, factory directly supply to clients, lower prices, more competitiveness.
What is the 3-allyl-2-[3-[3-allylbenzothiazol-2(3H)-ylidene]prop-1-enyl]benzothiazolium iodide ?
3-allyl-2-[3-[3-allylbenzothiazol-2(3H)-ylidene]prop-1-enyl]benzothiazolium iodide is , while it's Molecular Formula is C23H21 N2 S2 . I.
What is the CAS number for 3-allyl-2-[3-[3-allylbenzothiazol-2(3H)-ylidene]prop-1-enyl]benzothiazolium iodide ?
The CAS number of 3-allyl-2-[3-[3-allylbenzothiazol-2(3H)-ylidene]prop-1-enyl]benzothiazolium iodide is 34263-37-1.
More information of 3-allyl-2-[3-[3-allylbenzothiazol-2(3H)-ylidene]prop-1-enyl]benzothiazolium iodide 34263-37-1 are:
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Synonyms |
Benzothiazolium,3-(2-propenyl)-2-[3-[3-(2-propenyl)-2(3H)-benzothiazolylidene]-1-propenyl]-,iodide (9CI); Benzothiazolium,3-allyl-2-[3-(3-allyl-2-benzothiazolinylidene)propenyl]-, iodide (8CI);3,3'-Diallylthiacarbocyanine iodide |
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CAS?Number |
34263-37-1 |
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Molecular Formula |
C23H21 N2 S2 . I |
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Molecular Weight |
516.47 |
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Density |
g/cm3 |
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Boiling Point |
°Cat760mmHg |
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Flash Point |
°C |
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PSA |
65.29000 |
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LogP |
2.35600 |
What is 3-allyl-2-[3-[3-allylbenzothiazol-2(3H)-ylidene]prop-1-enyl]benzothiazolium iodide (34263-37-1) used for?
3-allyl-2-[3-[3-allylbenzothiazol-2(3H)-ylidene]prop-1-enyl]benzothiazolium iodide is a complex organic compound with the chemical formula C24H20N2S2I. It is a derivative of benzothiazolium, featuring a benzothiazolium core with an allyl group at the 3-position and a prop-1-enyl chain with a 3-allylbenzothiazol-2(3H)-ylidene group at the 2-position. 3-allyl-2-[3-[3-allylbenzothiazol-2(3H)-ylidene]prop-1-enyl]benzothiazolium iodide is characterized by its unique structure, which includes a conjugated system of double bonds and a heterocyclic ring system. It is typically synthesized through a series of chemical reactions involving allylation and condensation processes. Due to its specific structure, 3-allyl-2-[3-[3-allylbenzothiazol-2(3H)-ylidene]prop-1-enyl]benzothiazolium iodide may have potential applications in various fields, such as organic synthesis, materials science, or as a precursor in the development of new pharmaceuticals. However, its exact uses and properties would require further investigation and characterization.
InChI:InChI=1/C23H21N2S2/c1-3-16-24-18-10-5-7-12-20(18)26-22(24)14-9-15-23-25(17-4-2)19-11-6-8-13-21(19)27-23/h3-15H,1-2,16-17H2/q+1
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