4-Aminobenzo-2,1,3-thiadiazole Chemical Properties

Melting point:

67-69 °C (lit.)

Boiling point:

303.0±15.0 °C(Predicted)

Density 

1.485±0.06 g/cm3(Predicted)

storage temp. 

Keep in dark place,Inert atmosphere,Room temperature

form 

powder to crystal

pka

0.81±0.10(Predicted)

color 

Light yellow to Amber to Dark green

Water Solubility 

Insoluble in water.

BRN 

3551

CAS DataBase Reference

767-64-6(CAS DataBase Reference)

NIST Chemistry Reference

4-Amino-2,1,3-benzothiadiazole(767-64-6)

Safety Information

Hazard Codes 

Xn,Xi

Risk Statements 

22-36/37/38-20/21/22

Safety Statements 

22-26-36/37/39

RIDADR 

2811

WGK Germany 

3

RTECS 

DK9950000

HS Code 

2934.99.4400

HazardClass 

IRRITANT

PackingGroup 

III

MSDS

• Language:English Provider:4-Aminobenzo-2,1,3-thiadiazole
• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

4-Aminobenzo-2,1,3-thiadiazole Usage And Synthesis

Chemical Properties

white to light yellow crystal powder

Uses

4-Aminobenzo-2,1,3-thiadiazole is used in a study to synthesize and evaluate the inhibitory activity of a series of substituted benzimidazoles and small benzothiadiazoles on rat liver methionine synthase. It was used as potential levelers for Cu plating in submicrometer trenches.

Uses

4-Amino-2,1,3-benzothiadiazole was used in a study to synthesize and evaluate the inhibitory activity of a series of substituted benzimidazoles and small benzothiadiazoles on rat liver methionine synthase. It was used as potential levelers for Cu plating in submicrometer trenches.

General Description

4-Amino-2,1,3-benzothiadiazole is a gold green to yellow brown powder. It undergoes palladium catalyzed C-N coupling with 2-(2′-bromo-9′,9′-diethylfluoren-7′-yl)-9,9-diethylfluorene to form novel fluorescent dyes. 4-Amino-2,1,3-benzothiadiazole forms dicopper complexes.

4-Aminobenzo-2,1,3-thiadiazole(767-64-6)Related Product Information

• Sulfanilic acid
• Methyl anthranilate
• 2-Mercapto-5-methyl-1,3,4-thiadiazole
• 4,4'-Diaminodiphenylsulfone
• 4-Aminobenzoic acid
• Bis(2-ethylhexyl)amine
• Aniline
• 2,1,3-Benzothiadiazole
• p-Anisidine
• Diethanolamine
• Anthranilic acid
• 5-CHLORO-4-NITRO-2,1,3-BENZOTHIADIAZOLE
• 4-NITRO-2,1,3-BENZOTHIADIAZOLE
• COCO AMINE
• 5-METHYL-BENZO[1,2,5]THIADIAZOL-4-YLAMINE
• 5-METHYL-4-NITRO-2,1,3-BENZOTHIADIAZOLE
• 2,1,3-BENZOTHIADIAZOLE-4,5-DIAMINE
• 4-AMINO-5-CHLORO-1,2,3-BENZOTHIADIAZOLE