ChemicalBook > Product Catalog > Organic Chemistry > Aldehydes > 1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde
1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde
1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde Basic information
- Product Name:
- 1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde
- Synonyms:
-
- 1-(tert-butoxycarbonyl)-4-formylpiperidine
- 1-BOC-4-FORMYLPIPERIDINE 95%
- 1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde
- Piperidine-4-carboxaldehyde, N-BOC protected
- TERT-BUTYL 4-FORMYLPIPERIDINE-1-CARBOXYLATE
- 1-Piperidinecarboxylic acid, 4-formyl-, 1,1-dimethylethyl ester
- 1-TERT-BUTOXYCARBONYLPIPERIDINE-4-CARBOXALDEHYDE
- tert-Butyl 4-formyl-1-piperidinecarboxylate
- CAS:
- 137076-22-3
- MF:
- C11H19NO3
- MW:
- 213.27
- EINECS:
- 203-107-6
- Product Categories:
-
- C11
- Chemical Synthesis
- Piperidine
- Heterocyclic Building Blocks
- Organic Building Blocks
- Piperidines
- Carbonyl Compounds
- Heterocycles
- pharmacetical
- Aldehydes
- Pyrans, Piperidines & Piperazines
- Inhibitors
- Building Blocks
- C10-C12
- Mol File:
- 137076-22-3.mol
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1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde Chemical Properties
- Melting point:
- 34-40℃
- Boiling point:
- 295.4±33.0 °C(Predicted)
- Density
- 1.114±0.06 g/cm3(Predicted)
- Flash point:
- >110℃
- storage temp.
- 2-8°C
- solubility
- Soluble in methanol.
- pka
- -2.13±0.40(Predicted)
- form
- Oil
- color
- Clear Yellow
- Sensitive
- Air Sensitive
- InChIKey
- JYUQEWCJWDGCRX-UHFFFAOYSA-N
- CAS DataBase Reference
- 137076-22-3(CAS DataBase Reference)
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Safety Information
- Hazard Codes
- Xi,N,Xn
- Risk Statements
- 36/37/38-50-22
- Safety Statements
- 26-36/37/39-61
- RIDADR
- UN 3077 9/PG 3
- HS Code
- 29333990
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1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde Usage And Synthesis
Chemical Properties
Clear Yellow Oil
Uses
Reactant for synthesis of:• ;Pim-1 inhibitors1• ;Selective GPR119 agonists for type II diabetes2• ;M-tropic (R5) HIV-1 replication inhibitors3• ;HDAC inhibitors4• ;Selective 5-HT6 antagonists5Reactant for three-component vinylogous Mannich reactions6
Uses
1-Boc-piperidine-4-carboxaldehyde is used as reactant for synthesis of Pim-1 inhibitors, selective GPR119 agonists for type II diabetes, M-tropic (R5) HIV-1 replication inhibitors, HDAC inhibitors and selective 5-HT6 antagonists. It is also used as reactant for three-component vinylogous Mannich reactions
Uses
An intermediate for polycyclic indazole derivatives that are ERK inhibitors.
1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde Preparation Products And Raw materials
Raw materials
1-tert-Butoxycarbonyl-4-piperidinecarboxaldehydeSupplier
Shanghai Chemical Pharm-Intermediate Tech.Co., Ltd. Gold
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Shanghai Hobor Chemical Co., Ltd Gold
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Wuxi Kehua Biological Technology Co., Ltd. Gold
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Jiangsu Aikon Biopharmaceutical R&D co.,Ltd. Gold
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- 025-66113011 18112977050
- cb6@aikonchem.com
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1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde(137076-22-3)Related Product Information
- TERT-BUTYL 4-(AMINOCARBONYL)TETRAHYDROPYRIDINE-1(2H)-CARBOXYLATE
- N-Boc-Piperidine-4-carboxylic acid methyl ester
- 1-TERT-BUTYL 2-METHYL PIPERIDINE-1,2-DICARBOXYLATE
- N-BOC-3-Aminopiperidine
- 1-BOC-3-PIPERIDINECARBOXALDEHYDE
- N-Boc-4-piperidinemethanol
- (+/-)-1-N-BOC-PIPERIDINE-2-CARBOXAMIDE
- N-BOC-piperidine-4-carboxylic acid
- N-Boc-2-piperidinecarboxylic acid
- Ethyl N-Boc-piperidine-4-carboxylate
- Ethyl 1-Boc-piperidine-2-carboxylate
- 1-Boc-3-hydroxypiperidine
- N-Boc-piperidine-3-methanol
- N-Boc-piperidine-2-methanol
- 1-Boc-4-Methylaminopiperidine
- 1-N-BOC-PIPERIDINE-3-CARBOXAMIDE
- 1-Boc-3-piperidone
- N-(tert-Butoxycarbonyl)-4-piperidone