Introduction:Basic information about CAS 136-95-8|Benzo[d]thiazol-2-amine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Benzo[d]thiazol-2-amine |
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| CAS Number | 136-95-8 | Molecular Weight | 150.201 |
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| Density | 1.4±0.1 g/cm3 | Boiling Point | 307.5±25.0 °C at 760 mmHg |
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| Molecular Formula | C7H6N2S | Melting Point | 126-129 °C(lit.) |
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| MSDS | ChineseUSA | Flash Point | 139.8±23.2 °C |
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| Symbol | GHS07 | Signal Word | Warning |
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Names
| Name | 2-Benzothiazolamine |
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| Synonym | More Synonyms |
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Benzo[d]thiazol-2-amine BiologicalActivity
| Description | Benzo[d]thiazol-2-amine is a favorable ligand to synthesize dinuclear complexes which contain nitrogen heterocycle[1]. |
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| Related Catalog | Research Areas >>OthersSignaling Pathways >>Others >>Others |
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Chemical & Physical Properties
| Density | 1.4±0.1 g/cm3 |
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| Boiling Point | 307.5±25.0 °C at 760 mmHg |
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| Melting Point | 126-129 °C(lit.) |
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| Molecular Formula | C7H6N2S |
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| Molecular Weight | 150.201 |
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| Flash Point | 139.8±23.2 °C |
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| Exact Mass | 150.025162 |
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| PSA | 67.15000 |
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| LogP | 1.89 |
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| Vapour Pressure | 0.0±0.7 mmHg at 25°C |
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| Index of Refraction | 1.763 |
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| InChIKey | UHGULLIUJBCTEF-UHFFFAOYSA-N |
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| SMILES | Nc1nc2ccccc2s1 |
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| Water Solubility | <0.1 g/100 mL at 19 ºC |
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Toxicological Information
CHEMICAL IDENTIFICATION - RTECS NUMBER :
- DL1050000
- CHEMICAL NAME :
- Benzothiazole, 2-amino-
- CAS REGISTRY NUMBER :
- 136-95-8
- LAST UPDATED :
- 199701
- DATA ITEMS CITED :
- 5
- MOLECULAR FORMULA :
- C7-H6-N2-S
- MOLECULAR WEIGHT :
- 150.21
- WISWESSER LINE NOTATION :
- T56 BN DSJ CZ
HEALTH HAZARD DATAACUTE TOXICITY DATA - TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- >1 gm/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intraperitoneal
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 200 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intravenous
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 126 mg/kg
- TOXIC EFFECTS :
- Details of toxic effects not reported other than lethal dose value
MUTATION DATA - TYPE OF TEST :
- Mutation in microorganisms
- TEST SYSTEM :
- Bacteria - Salmonella typhimurium
- DOSE/DURATION :
- 2500 ug/plate
- REFERENCE :
- FCTOD7 Food and Chemical Toxicology. (Pergamon Press Inc., Maxwell House, Fairview Park, Elmsford, NY 10523) V.20- 1982- Volume(issue)/page/year: 23,695,1985
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Safety Information
| Symbol | GHS07 |
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| Signal Word | Warning |
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| Hazard Statements | H302 |
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| Precautionary Statements | P301 + P312 + P330 |
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| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
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| Hazard Codes | Xn:Harmful |
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| Risk Phrases | R22;R36 |
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| Safety Phrases | S26 |
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| RIDADR | UN 2811 6.1/PG 3 |
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| WGK Germany | 2 |
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| RTECS | DL1050000 |
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| Hazard Class | 6.1 |
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| HS Code | 2934200090 |
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Customs
| HS Code | 2934999090 |
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| Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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Articles7
More Articles
| Synthesis, antioxidant properties and radioprotective effects of new benzothiazoles and thiadiazoles. Bioorg. Med. Chem. 17 , 5275-84, (2009) In this work, we report the synthesis and characterization of new compounds derived from benzothiazoles and thiadiazoles. We observed that structural modifications on these skeletons affected the anti... | |
| Simultaneous determination of benzothiazoles, benzotriazoles and benzosulfonamides by solid phase microextraction-gas chromatography-triple quadrupole mass spectrometry in environmental aqueous matrices and human urine J. Chromatogr. A. 1338 , 164-73, (2014) • Benzothiazoles, benzotriazoles and benzosulfonamides determination in aqueous matrices. • New environmental-friendly and high-throughput protocol developed by SPME-GC-QqQMS. • Sample preparation str... | |
| Virtual screening identification of nonfolate compounds, including a CNS drug, as antiparasitic agents inhibiting pteridine reductase. J. Med. Chem. 54 , 211-221, (2011) Folate analogue inhibitors of Leishmania major pteridine reductase (PTR1) are potential antiparasitic drug candidates for combined therapy with dihydrofolate reductase (DHFR) inhibitors. To identify n... | |
Synonyms
| Benzo[d]thiazol-2-amine |
| 2-Benzothiazolamine |
| 2-Aminobenzothiazole |
| Benzothiazole-2-ylamine |
| 1,3-Benzothiazol-2-amine |
| EINECS 205-268-4 |
| MFCD00005785 |