ChemicalBook--->CAS DataBase List--->19155-88-5

19155-88-5

19155-88-5 Structure

19155-88-5 Structure
IdentificationMore
[Name]

2,1,3-Benzoxadiazole-5-carboxylic acid
[CAS]

19155-88-5
[Synonyms]

2,1,3-BENZOXADIAZOLE-5-CARBOXYLIC ACID
BENZOFURAZAN-5-CARBOXYLIC ACID
BUTTPARK 29\08-25
RARECHEM AL BO 0811
1,2,3-Benzoxadiazole-5-carboxylicacid
2,1,3-Benzoxadiazole-5-Carboxylic acid, HPLC 97%
[EINECS(EC#)]

670-648-2
[Molecular Formula]

C7H4N2O3
[MDL Number]

MFCD00276977
[Molecular Weight]

164.12
[MOL File]

19155-88-5.mol
Chemical PropertiesBack Directory
[Melting point ]

157-160 °C (lit.)
[Boiling point ]

360.0±34.0 °C(Predicted)
[density ]

1.558±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder
[pka]

3.10±0.30(Predicted)
[color ]

Yellow
[CAS DataBase Reference]

19155-88-5(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

29349990
Hazard InformationBack Directory
[Chemical Properties]

Light yellow powder
[Synthesis]

BENZOFUROXAN-5-CARBOXYLIC ACID

6086-24-4

2,1,3-Benzoxadiazole-5-carboxylic acid

19155-88-5

General procedure for the synthesis of 2,1,3-benzoxadiazole-5-carboxylic acid from benzoxafurazan-5-carboxylic acid: 2,1,3-benzoxadiazole-5-carboxylic acid N-oxide (80 g) was dissolved in anhydrous ethanol (800 ml) in a 2 L reactor fitted with a mechanical stirrer, a thermometer, a dosing funnel, a reflux condenser and a nitrogen inlet. Triethyl phosphite (114.05 g) was slowly added to this solution over a period of 10 minutes at a temperature range of 62°C to 70°C. The reaction mixture was heated to reflux temperature (76-78°C) and maintained for 2 hours. The progress of the reaction was monitored by thin layer chromatography (TLC, unfolding reagent ratio of CHCl3:acetone:acetic acid = 100:2:1) to confirm that the reaction was complete. Subsequently, the solvent was evaporated under reduced pressure conditions (30 mbar, 40 °C) to give a black oily product (180 g). To this oily product, water (400 ml) was added and subsequently extracted with ethyl acetate (first 400 ml, second 160 ml). The organic phases were combined and washed with 850 ml of aqueous sodium hydroxide (9.5 μl).

[References]

[1] Patent: EP2187888, 2015, B1. Location in patent: Paragraph 0087; 0089
[2] MedChemComm, 2015, vol. 6, # 9, p. 1673 - 1678
[3] Journal of Medicinal Chemistry, 1968, vol. 11, # 2, p. 305 - 311
Spectrum DetailBack Directory
[Spectrum Detail]

2,1,3-Benzoxadiazole-5-carboxylic acid(19155-88-5)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2,1,3-benzoxadiazole-5-carboxylic acid(19155-88-5)
[Sigma Aldrich]

19155-88-5(sigmaaldrich)
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