HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 16237421, compound → HCID 66830863, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 16237421 | HCID 16237421 | — |
| Reactant | HCID 66830866 | HCID 66830866 | — |
| Reactant | HCID 66830876 | HCID 66830876 | — |
| Reactant | HCID 66830885 | HCID 66830885 | — |
| Product | HCID 66830863 | HCID 66830863 | 22% |
Reaction Steps
Furthermore, 4-((3-(3-carboxyhexyl)benzo[d]thiazole-2(3H)-ylidene) methyl)-1-methylquinoliniumbromide with a linker (a polymethylene chain linked to a carboxyl group) having a carbon number n of 6 was synthesized from the mixture of 3-(4-carboxyhexyl)-2-methylbenzothiazolium bromide and 2-methylbenzothiazolium bromide by the same method as that used for Compound 107, which was obtained with a yield of 22%. The instrumental analytical values are indicated below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383792B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-c080e6539e5a479fbaacbf2380f1b1ed |
| Source note | uspto-grants-2013_02 |