| Identification | More | [Name]
2-Amino-6-nitrobenzothiazole | [CAS]
6285-57-0 | [Synonyms]
2-AMINO-6-NITROBENZOTHIAZOLE
6-NITRO-1,3-BENZOTHIAZOL-2-AMINE
6-NITRO-2-AMINOBENZOTHIAZOLE
6-NITRO-2-BENZOTHIAZOLAMINE
6-NITRO-BENZOTHIAZOL-2-YLAMINE
IFLAB-BB F1386-0392
LABOTEST-BB LT00454107
6-nitro-2-benzothiazolamin
6-nitro-1,3-benzothiazol-2-ylamine
6-nitrobenzothiazol-2-amine
6-Nitrobenzo[d]thiazol-2-amine
2-AMINO-6-NITROBENZOTHIAZOLE, 97+%
2-Amino-6-NitroBenzothiazole(Nabtho)
2-Benzothiazolamine,6-nitro-(9CI)
2-Amino-6-nitrobenzothiazol | [EINECS(EC#)]
228-513-7 | [Molecular Formula]
C7H5N3O2S | [MDL Number]
MFCD00005786 | [Molecular Weight]
195.2 | [MOL File]
6285-57-0.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [RIDADR ]
UN 2811 6.1/PG 3
| [WGK Germany ]
2
| [RTECS ]
DL0865000
| [TSCA ]
Yes | [HazardClass ]
6.1 | [PackingGroup ]
III | [HS Code ]
29342000 |
| Hazard Information | Back Directory | [General Description]
Orange crystals or yellow powder. | [Reactivity Profile]
2-AMINO-6-NITROBENZOTHIAZOLE(6285-57-0) is incompatible with strong oxidizing agents and strong acids. | [Air & Water Reactions]
Insoluble in water. | [Fire Hazard]
Flash point data for this compound are not available; however, 2-AMINO-6-NITROBENZOTHIAZOLE is probably combustible. | [Chemical Properties]
yellow crystalline powder | [Uses]
2-Amino-6-nitrobenzothiazole has been used:
- as model analyte for voltammetric determination of electrochemically reducible organic substances
- in the synthesis of 2-methyl-4-nitro-2H-pyrazole-3-carboxylic acid[2-(cyclohexanecarbonylamino)benzothiazol-6-yl]amide derivatives
- in the preparation of push-pull nonlinear optical chromophores containing thiazole and benzothiazole acceptors
- as a base in dye production by diazotation reaction
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