Ticlatone structure
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Common Name | Ticlatone | ||
|---|---|---|---|---|
| CAS Number | 70-10-0 | Molecular Weight | 185.63100 | |
| Density | 1.515 g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C7H4ClNOS | Melting Point | 270-272ºC | |
| MSDS | N/A | Flash Point | N/A | |
Use of TiclatoneTiclatone is an antifungal that can be used for the research of mycoses[1]. |
| Name | 6-chloro-1,2-benzothiazol-3-one |
|---|---|
| Synonym | More Synonyms |
| Description | Ticlatone is an antifungal that can be used for the research of mycoses[1]. |
|---|---|
| Related Catalog | |
| References |
| Density | 1.515 g/cm3 |
|---|---|
| Melting Point | 270-272ºC |
| Molecular Formula | C7H4ClNOS |
| Molecular Weight | 185.63100 |
| Exact Mass | 184.97000 |
| PSA | 61.10000 |
| LogP | 2.24300 |
| Index of Refraction | 1.669 |
| InChIKey | POPOYOKQQAEISW-UHFFFAOYSA-N |
| SMILES | O=c1[nH]sc2cc(Cl)ccc12 |
| Storage condition | 2-8°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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| HS Code | 2934999090 |
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~95%
Ticlatone CAS#:70-10-0 |
| Literature: Sumitomo Seika Chemicals Co., Ltd.; HIYAMA, Takehiro; YOKOE, Ichiro; TAKEUCHI, Takeshi; SUZUKI, Michio Patent: EP2687519 A1, 2014 ; Location in patent: Paragraph 0047; 0048 ; |
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~%
Ticlatone CAS#:70-10-0 |
| Literature: Journal of Organic Chemistry, , vol. 53, # 12 p. 2850 - 2852 |
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~%
Ticlatone CAS#:70-10-0 |
| Literature: Journal of Organic Chemistry, , vol. 53, # 12 p. 2850 - 2852 |
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~%
Ticlatone CAS#:70-10-0 |
| Literature: Heterocycles, , vol. 51, # 12 p. 3005 - 3012 |
| Precursor 1 | |
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| DownStream 1 | |
| HS Code | 2934999090 |
|---|---|
| Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
| 6-chlorobenzisothiazolinone |
| 6-CHLORO-1,2-BENZISOTHIAZOL-3(2H)-ONE |
| Ticlatonum [INN-Latin] |
| 6-Chlor-3-oxo-2,3-dihydro-benzisothiazol |
| TICLATONE |
| 6-chloro-1,2-benzisothiazol-3-one |
| 6-chlorobenzo[d]isothiazol-3-one |
| Ticlatone [USAN:INN] |
| Landromil |
| Ticlatona [INN-Spanish] |
| 6-chloro-1,2-benzisothiazolin-3-one |
| Fer 1443 |
| 6-Chloro-1,2-benzisothiazolone |