ChemicalBook--->CAS DataBase List--->874-37-3

874-37-3

874-37-3 Structure

874-37-3 Structure
IdentificationBack Directory
[Name]

2,1,3-BENZOTHIADIAZOL-5-AMINE
[CAS]

874-37-3
[Synonyms]

NSC 231627
BUTTPARK 95\50-71
piazthiol-5-ylamine
2,1,3-BENZOTHIADIAZOL-5-AMINE
2,1,3-benzothiadiazol-6-amine
5-Amino-2,1,3-benzothiadiazole
BENZO[1,2,5]THIADIAZOL-5-YLAMINE
benzo[c][1,2,5]thiadiazol-5-aMine
(2,1,3-Benzothiadiazol-5-yl)amine
2,1,3-Benzothiadiazol-5-amine ,97%
2,1,3-benzothiadiazol-5-amine(SALTDATA: FREE)
[Molecular Formula]

C6H5N3S
[MDL Number]

MFCD00185826
[MOL File]

874-37-3.mol
[Molecular Weight]

151.19
Chemical PropertiesBack Directory
[Melting point ]

112-115
[Boiling point ]

303.0±15.0 °C(Predicted)
[density ]

1.485±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

1.75±0.47(Predicted)
[Appearance]

Yellow to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P260-P280-P312
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[Hazard Note ]

Harmful
[HazardClass ]

IRRITANT
[HS Code ]

2934999090
Hazard InformationBack Directory
[Uses]

2,1,3-benzothiadiazol-5-amine is a useful research chemical, a benzothiadiazole derivative with pesticidal properties. An anti-viral and antibacterial agent.
[Synthesis]

5-NITRO-2,1,3-BENZOTHIADIAZOLE

16252-88-3

2,1,3-BENZOTHIADIAZOL-5-AMINE

874-37-3

5-Nitrobenzo[c][1,2,5]thiadiazole (Compound 16, 2 g, 11.04 mmol) was used as a raw material, which was dissolved in a mixed solvent of ethanol and water (2:1, 3 mL, v/v) with NH4Cl (2.34 g, 44.20 mmol). The reaction mixture was placed in an oil bath at 90°C and refluxed for 30 min. Subsequently, iron powder (2.47 g, 44.20 mmol) was added to the reaction system and the reaction continued to be stirred under reflux conditions for 3 hours. After the completion of the reaction was monitored by TLC, the hot reaction mixture was filtered and the residue was washed with ethanol. The filtrates were combined, neutralized with saturated NaHCO3 solution and then extracted with ethyl acetate. The organic phase was dried with anhydrous sodium sulfate and concentrated to give the target product 2,1,3-benzothiazol-5-amine (Compound 17, 1.5 g, 90.3% yield).

[References]

[1] Patent: CN108341791, 2018, A. Location in patent: Paragraph 0142; 0143; 0145
[2] Patent: US6420567, 2002, B1
[3] Zhurnal Obshchei Khimii, 1955, vol. 25, p. 199,209; engl. Ausg. S. 183, 190
[4] Zhurnal Obshchei Khimii, 1954, vol. 24, p. 133,134; engl. Ausg. S. 131
[5] Zhurnal Obshchei Khimii, 1958, vol. 28, p. 20,25; engl. Ausg. S. 20, 24
Spectrum DetailBack Directory
[Spectrum Detail]

2,1,3-BENZOTHIADIAZOL-5-AMINE(874-37-3)1HNMR
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