Basic information Application Safety Supplier Related

1-METHYL-1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLIC ACID

Basic information Application Safety Supplier Related

1-METHYL-1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLIC ACID Basic information

Product Name:
1-METHYL-1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLIC ACID
Synonyms:
  • 1-METHYL-1H-BENZOTRIAZOLE-5-CARBOXYLIC ACID
  • 1-METHYL-1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLIC ACID
  • 1-methyl-1H-benzo[d][1,2,3]triazole-5-carboxylic acid
  • 1H-Benzotriazole-5-carboxylicacid, 1-Methyl-
  • 1-methylbenzotriazole-5-carboxylic acid
  • 1,2,3-Propanetriol,1,8-diacetate
  • 1-methyl-1H-1,2,3-benzotriazole-5-carboxylic acid - [M86437]
CAS:
305381-67-3
MF:
C8H7N3O2
MW:
177.16
Mol File:
305381-67-3.mol
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1-METHYL-1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLIC ACID Chemical Properties

Melting point:
250 °C
Boiling point:
432.4±18.0 °C(Predicted)
Density 
1.49±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
3.51±0.30(Predicted)
Appearance
Off-white to light brown Solid
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Safety Information

Hazard Codes 
Xi
Risk Statements 
41
Hazard Note 
Harmful
HS Code 
2933998090
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1-METHYL-1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLIC ACID Usage And Synthesis

Application

1-Methyl-1,2,3-benzotriazole-5-carboxylic acid is an organic intermediate that can be prepared from 4-amino-3-nitrobenzoic acid as a raw material. 4-amino-3-nitrobenzoic acid is then prepared, followed by methylation to obtain methyl 4-methylamino-3-nitrobenzoate, reduction of the nitro group to obtain methyl 4-methylamino-3-aminobenzoate, cyclization to obtain methyl 4-methylamino-3-aminobenzoate, and finally hydrolysis of the methyl ester to obtain 1-methyl-1,2,3-benzotriazole-5-carboxylic acid.

Synthesis

The synthesis of 1-Methyl-1H-1,2,3-benzotriazole-5-carboxylic acid is carried out as follows:
To a stirred suspension of the diamine 280 (1.08g; 6.48mmol) (or any other oarylenediamine) in water (25 mL) at 0°C, concentrated HCl (5.4 mL) was added drop wise followed by slow addition of a solution of NaNO2 (643mg; 9.3mmol) in water (10 mL). The reaction mixture was stirred at 0°C for 2h and then was allowed to warm up to 10°C over 4h; neutralized with a solution of KOH (5.6 g) in water (30mL) (final pH = 6); concentrated and purified by preparative HPLC in reverse phase mode (column aquasil C-18, elution 5% to 95% MeOH in water), to afford the title compound 284 (211 mg; 18% yield). 1-Methyl-1H-benzo[d][1,2,3]triazole-5-carboxylic acid (284), yield (211 mg; 18%). 1HNMR: (400.2 MHz, DMSO) δ (ppm): 8.35 (s; 1H); 8.08 (dd, J= 1.4, 8.6 Hz; 1H); 7.75 (d, J= 1.4 Hz; 1H); 4.03 (s, 3H). MS: calc: 177.1; found: 178.1 (M+H).

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