ChemicalBook > CAS DataBase List > 2H-1,2,3 TRIAZOLE-2-ACETIC ACID

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
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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
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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.

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N-Bromosuccinimide Price

TRC
Product number
T767523
Product name
2H-1,2,3-Triazole-2-aceticAcid
Packaging
100mg
Price
$45
Updated
2021/12/16
TRC
Product number
T767523
Product name
2H-1,2,3-Triazole-2-aceticAcid
Packaging
1g
Price
$310
Updated
2021/12/16
AK Scientific
Product number
W6268
Product name
2H-1,2,3-Triazole-2-aceticacid
Packaging
5g
Price
$317
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA154156
Product name
2H-1,2,3Triazole-2-acetic acid
Packaging
2g
Price
$494
Updated
2021/12/16
Matrix Scientific
Product number
076486
Product name
2H-1,2,3-Triazole-2-acetic acid
Purity
95+%
Packaging
1g
Price
$500
Updated
2021/12/16
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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

Raw materials

Preparation Products

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