(4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE
- Product Name
- (4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE
- CAS No.
- 218772-96-4
- Chemical Name
- (4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE
- Synonyms
- 4-piperidon-1-acetic acid;1-Piperidineacetic acid, 4-oxo-;2-(4-Oxo-1-piperidyl)acetic Acid;2-(4-Oxopiperidin-1-yl)acetic acid;2-(4-oxo-1-piperidinyl)acetic acid hydrochloride;(4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE
- CBNumber
- CB0253716
- Molecular Formula
- C7H11NO3
- Formula Weight
- 157.17
- MOL File
- 218772-96-4.mol
(4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE Property
- storage temp.
- Sealed in dry,Room Temperature
Safety
- HazardClass
- IRRITANT
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
- O847213
- Product name
- (4-Oxo-piperidin-1-yl)-aceticAcid
- Packaging
- 100mg
- Price
- $90
- Updated
- 2021/12/16
- Product number
- 034050
- Product name
- (4-Oxo-piperidin-1-yl)-acetic acid hydrochloride
- Packaging
- 1g
- Price
- $378
- Updated
- 2021/12/16
- Product number
- CHM0081242
- Product name
- (4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE
- Purity
- 95.00%
- Packaging
- 500MG
- Price
- $796.95
- Updated
- 2021/12/16
- Product number
- A116748
- Product name
- 2-(4-Oxopiperidin-1-yl)aceticacid
- Purity
- 95+%
- Packaging
- 5g
- Price
- $845
- Updated
- 2021/12/16
- Product number
- CM122545
- Product name
- 2-(4-oxopiperidin-1-yl)aceticacid
- Purity
- 95%
- Packaging
- 5g
- Price
- $954
- Updated
- 2021/12/16
(4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE Chemical Properties,Usage,Production
Synthesis
5292-43-3
40064-34-4
218772-96-4
Step 1. 4-Piperidone monohydrate hydrochloride (5 g, 0.033 mol) was mixed with tert-butyl bromoacetate (6.98 g, 0.037 mol) and potassium carbonate (13.65 g, 0.099 mol) in dimethylformamide (100 ml) and reacted for 24 hours at 100 °C. After completion of the reaction, the mixture was cooled and concentrated in vacuum. The residue was partitioned between saturated potassium carbonate solution and ether (2 x 50 ml). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and evaporated to dryness to give 7.36 g of tert-butyl 2-(4-oxopiperidin-1-yl)acetate in 94% yield. The product was characterized by 1H NMR (CDCl3): δ 1.45 (9H, s), 2.45 (4H, t, J=7Hz), 2.3-2.4 (4H, m), 3.29 (2H, s).
References
[1] Patent: US6281226, 2001, B1
(4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE Preparation Products And Raw materials
Raw materials
Preparation Products
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