2H-1,2,3 TRIAZOLE-2-ACETIC ACID
- Product Name
- 2H-1,2,3 TRIAZOLE-2-ACETIC ACID
- CAS No.
- 4320-91-6
- Chemical Name
- 2H-1,2,3 TRIAZOLE-2-ACETIC ACID
- Synonyms
- AP8Impurity;2H-1,2,3 TRIAZOLE-2-ACETIC ACID;2-(2H-1,2,3-triazol-2-yl)acetic acid
- CBNumber
- CB4458252
- Molecular Formula
- C4H5N3O2
- Formula Weight
- 127.1
- MOL File
- 4320-91-6.mol
2H-1,2,3 TRIAZOLE-2-ACETIC ACID Property
- Boiling point:
- 344.0±44.0 °C(Predicted)
- Density
- 1.53±0.1 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 2?+-.0.10(Predicted)
- Appearance
- Off-white to light yellow Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- T767523
- Product name
- 2H-1,2,3-Triazole-2-aceticAcid
- Packaging
- 100mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- T767523
- Product name
- 2H-1,2,3-Triazole-2-aceticAcid
- Packaging
- 1g
- Price
- $310
- Updated
- 2021/12/16
- Product number
- W6268
- Product name
- 2H-1,2,3-Triazole-2-aceticacid
- Packaging
- 5g
- Price
- $317
- Updated
- 2021/12/16
- Product number
- FA154156
- Product name
- 2H-1,2,3Triazole-2-acetic acid
- Packaging
- 2g
- Price
- $494
- Updated
- 2021/12/16
- Product number
- 076486
- Product name
- 2H-1,2,3-Triazole-2-acetic acid
- Purity
- 95+%
- Packaging
- 1g
- Price
- $500
- Updated
- 2021/12/16
2H-1,2,3 TRIAZOLE-2-ACETIC ACID Chemical Properties,Usage,Production
Synthesis
4320-90-5
4320-91-6
The general procedure for the synthesis of 2H-2-acetic acid-1,2,3-triazole-1,2,3-triazole from ethyl 2-(2H-1,2,3-triazol-2-yl)acetate was as follows: 1. Preparation of 2H-1,2,3-triazol-2-ylacetic acid: a solution of lithium hydroxide monohydrate (2.5 g, 60 mmol) in water (15 mL) was added to a solution of ethyl 2-(2H-1,2,3-triazol-2-yl)acetate (7.8 g, 50 mmol), and the reaction was stirred for 18 h at room temperature. 2. Upon completion of the reaction, the reaction mixture was acidified with 2M hydrochloric acid (150 mL) followed by extraction with dichloromethane (150 mL x 3). 3. The organic phases were combined, dried over magnesium sulfate and concentrated under reduced pressure to afford 2H-2-acetic acid-1,2,3-triazole as a white solid in 81% (5.2 g) yield. 4. 4. Product characterization: 1H NMR (400 MHz, CDCl3) δ: 5.35 (s, 2H), 7.72 (s, 2H); LRMS APCI m/z 128 [M + H]+.
References
[1] Patent: WO2006/123242, 2006, A1. Location in patent: Page/Page column 35
2H-1,2,3 TRIAZOLE-2-ACETIC ACID Preparation Products And Raw materials
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