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Acitazanolast

CAS No.
114607-46-4
Chemical Name:
Acitazanolast
Synonyms
MTCC;WP 871;CS-264;Zepenolast;Acitazanolast;WP-871; ZEPELIN;Acitazanolast.H2O;Acitazanolast/MTCC;Acitazanolast, >=98%;ACITAZANOLAST 114607-46-4
CBNumber:
CB71177957
Molecular Formula:
C9H7N5O3
Molecular Weight:
233.18
MDL Number:
MFCD00872322
MOL File:
114607-46-4.mol
MSDS File:
SDS
Last updated:2023-09-20 16:43:00

Acitazanolast Properties

Melting point 241-243 °C (decomp)
Density 1.660±0.06 g/cm3(Predicted)
pka 2.05±0.20(Predicted)
FDA UNII 99Y8VJ356G

Acitazanolast price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biorbyt Ltd orb180759 Acitazanolast (WP-871,Zepelin) >98% 114607-46-4 100mg $615.4 2021-12-16 Buy
American Custom Chemicals Corporation API0007782 ACITAZANOLAST 95.00% 114607-46-4 10MG $675.15 2021-12-16 Buy
Medical Isotopes, Inc. 18445 Acitazanolast 114607-46-4 5mg $950 2021-12-16 Buy
Biorbyt Ltd orb180759 Acitazanolast (WP-871,Zepelin) >98% 114607-46-4 250mg $1208.7 2021-12-16 Buy
Matrix Scientific 132204 2-((3-(1H-Tetrazol-5-yl)phenyl)-amino)-2-oxoacetic acid 97% 114607-46-4 5g $1797 2021-12-16 Buy
Product number Packaging Price Buy
orb180759 100mg $615.4 Buy
API0007782 10MG $675.15 Buy
18445 5mg $950 Buy
orb180759 250mg $1208.7 Buy
132204 5g $1797 Buy

Acitazanolast Chemical Properties,Uses,Production

Originator

Zepelin ,Kowa

Uses

2-((3-(1H-Tetrazol-5-yl)phenyl)-amino)-2-oxoacetic acid is used in biological study to identify mechanisms-of-action targets for drugs and drug candidates as biological probes.

Definition

ChEBI: Acitazanolast is a member of tetrazoles.

Manufacturing Process

2 Methods of preparation of 3-(1H-tetrazol-5-yl)oxanilic acid:
1. 5.0 g of 3-(1H-tetrazol-5-yl)aniline was dissolved in 25 ml of N,Ndimethylformamide, followed by adding 5.68 g of triethylamine. Then, 5.64 g of ether oxalyl chloride was dropwise added to the solution while cooling in ice water. After completion of the dropwise addition, the reaction temperature was slowly raised up to room temperature and the reaction was continued for 15 h. After the reaction was completed, the reaction mixture was poured into 100 ml of ice water and crystals separated out from the solution was filtered off to obtain 8.3 g of ethyl 3-(1H-tetrazol-5-yl)oxanilate (yield 94.1%), melting point 192°-l93°C (recrystallized from acetone/n-hexane).
The ethyl 3-(1H-tetrazol-5-yl)oxanilate (5.0 g), was dissolved in 35 ml of ethanol and 100 ml of 0.5 N sodium hydroxide was dropwise added thereto under water cooling. After the dropwise addition, the reaction temperature was slowly raised up to room temperature and under such condition, the reaction was carried out for 3 h. This solution was dropwise added to 70 ml of 4 N hydrochloric acid at room temperature. Thereafter, the solution was stirred for 1 h and crystals separated out from the solution was filtered off. The resultant crystals were washed with water and 3.9 g of 3-(1H-tetrazol-5- yl)oxanilic acid was recovered (yield 87.4%), melting point 241°-243°C (dec. recrystallized from isopropyl).
2. Oxalyl chloride (12.0 g) was dissolved in 50 ml of anhydrous dimethoxyethane. To this solution a solution of 3-(1H-tetrazol-5-yl)aniline (5.0 g) in 250 ml of anhydrous dimethoxyethane was dropwise added over 3 h at room temperature while stirring. Insolubles were removed by filtering the solution, then 50 ml of water was gradually added to the reaction mixture under ice cooling and stirring was continued for 1 h at room temperature. Then, 500 ml of ethyl acetate was added thereto to carry out extraction, the extract was washed with water, dried over anhydrous sodium sulfate and then the solvent was distilled off to obtain 5.4 g of the 3-(1H-tetrazol-5- yl)oxanilic acid (yield 74.8%), melting point 241°-243°C (dec. recrystallized from isopropyl).

Therapeutic Function

Anti-asthmatic, Antiallergic, Bronchodilator

79-37-8
73732-51-1
114607-46-4
Synthesis of Acitazanolast from Oxalyl chloride and 5-(3-AMINOPHENYL)TETRAZOLE

Acitazanolast Preparation Products And Raw materials

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Aladdin Scientific
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Acitazanolast Spectrum

Oxo[[3-(1H-tetrazol-5-yl)phenyl]amino]acetic acid Oxo[3-(1H-tetrazole-5-yl)anilino]acetic acid Zepenolast Acitazanolast WP 871 2-(3-(1H-tetrazol-5-yl)phenylamino)-2-oxoacetic acid Acitazanolast, >=98% Acitazanolast.H2O 3-(1H-TETRAZOL-5-YL)-OXANILICACI MTCC N-[3-(1H-Tetrazol-5-yl)phenyl]oxamidic acid Acetic acid,2-oxo-2-[[3-(2H-tetrazol-5-yl)phenyl]amino]- ACITAZANOLAST; WP871; ZEPELIN;WP 871 CS-264 Acitazanolast (WP-871,Zepelin) WP-871; ZEPELIN ACITAZANOLAST 114607-46-4 Acitazanolast/MTCC 114607-46-4