CAS Number216854-23-8
Synonyms(S)-3-(BOC-Amino)piperidine; Carbamic acid, N-[(3S)-3-piperidinyl]-, 1,1-dimethylethyl ester; (S)-3-N-Boc-Aminopiperidine; (S)-3-(tert-Butoxycarbonylamino)piperidine; (S)-3-Boc-Aminopiperidine; (S)-tert-Butyl piperidin-3-ylcarbamate; MFCD03093383; 2-Methyl-2-propanyl (3S)-3-piperidinylcarbamate
Molecular FormulaC10H20N2O2
Molecular Weight200.28
Purity98%
Density1.0±0.1 g/cm3
Boiling Point304.8±31.0 °C at 760 mmHg
Melting Point122-127°C
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 216854-23-8 |
| Catalog No. | 2A-9000335 |
| Chinese Name | (S)-3-Boc-氨基哌啶 |
| Synonyms | (S)-3-(BOC-Amino)piperidine; Carbamic acid, N-[(3S)-3-piperidinyl]-, 1,1-dimethylethyl ester; (S)-3-N-Boc-Aminopiperidine; (S)-3-(tert-Butoxycarbonylamino)piperidine; (S)-3-Boc-Aminopiperidine; (S)-tert-Butyl piperidin-3-ylcarbamate; MFCD03093383; 2-Methyl-2-propanyl (3S)-3-piperidinylcarbamate |
| Molecular Formula | C10H20N2O2 |
| Molecular Weight | 200.28 |
| Purity | 98 |
| Density | 1.0±0.1 g/cm3 |
| Boiling Point | 304.8±31.0 °C at 760 mmHg |
| Melting Point | 122-127°C |
| Storage Condition | Storage: Sealed, cool, ventilated and dry |
| Application | (S)-3-Boc-aminopiperidine is a biochemical reagent that can be used as a biological material or organic compound in life science-related research. |
| HTC | 2933399090 |
| SMILES | CC(C)(C)OC(=O)NC1CCCNC1 |
| InChI Key | WUOQXNWMYLFAHT-QMMMGPOBSA-N |
| Hazard Symbols | Transport |
| Risk Codes | R37/38;R41 |
| Safety Description | S26;S39 |
| MSDS | msds/335_1_216854_23_8.pdf |
| Bioactivity | (S)-3-Boc-aminopiperidine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others Chemical & Physical Properties Density 1.0±0.1 g/cm3 Boiling Point 304.8±31.0 °C at 760 mmHg Melting Point 122-127°C Molecular Formula C10H20N2O2 Molecular Weight 200.28 Flash Point 138.2±24.8 °C Exact Mass 200.152481 PSA 50.36000 LogP 1.37 Vapour Pressure 0.0±0.6 mmHg at 25°C Index of Refraction 1.480 InChIKey WUOQXNWMYLFAHT-QMMMGPOBSA-N SMILES CC(C)(C)OC(=O)NC1CCCNC1 |
| Use of | (S)-3-Boc-aminopiperidine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Properties Name tert-butyl N-[(3S)-piperidin-3-yl]carbamate Synonym More Synonyms (S)-3-N-Boc-aminopiperidine Biological Activity Description (S)-3-Boc-aminopiperidine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others Chemical & Physical Properties Molecular Formula C10H20N2O2 Exact Mass 200.152481 PSA 50.36000 Index of Refraction 1.480 InChIKey WUOQXNWMYLFAHT-QMMMGPOBSA-N |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 20.0% |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available |
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