N-BOC-1,2,3,6-TETRAHYDROPYRIDINE Basic information
Product Name: | N-BOC-1, 2, 3, 6-TETRAHYDROPYRIDINE |
Synonyms: | N-TERT-BUTOXYCARBONYL-1, 2, 3, 6-TETRAHYDROPYRIDINE; N-BOC-1, 2, 3, 6-TETRAHYDROPYRIDINE; N-BOC-1, 2, 5, 6-TETRAHYDROPYRIDINE; 1-Boc-1, 2, 3, 6-tetrahydro-pyridine; 1, 2, 3, 6-Tetrahydropyridine, N-BOC protected; 3, 6-Dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester; Tert-butyl5, 6-dihydropyridine-1(2H)-carboxylate; tert-Butyl 3, 6-dihydropyridine-1(2H)-carboxylate |
CAS: | 85838-94-4 |
MF: | C10H17NO2 |
MW: | 183.25 |
EINECS: | |
Product Categories: | Heterocycle-Pyridine series |
Mol File: | 85838-94-4.mol |
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N-BOC-1,2,3,6-TETRAHYDROPYRIDINE Chemical Properties
Boiling point | 78-84℃/5mm |
Boiling Point: | 241.5ºC at 760 mmHg |
Flash Point: | 99.9ºC |
density | 1.029 g/cm3 |
refractive index | 1.4650 to 1.4690 |
Water Solubility | Insoluble in water. Soluble in organic solvents. |
Safety Information
Hazard Codes | Xi,T |
Risk Statements | 36/37/38-25 |
Safety Statements | 26-36/37/39-45 |
HazardClass | IRRITANT |
Hs code | 2933399090 |
MSDS Information
N-BOC-1,2,3,6-TETRAHYDROPYRIDINE Usage And Synthesis
Chemical Properties | Liquid |
Description | tert-Butyl 1, 2, 3, 6-Tetrahydro-1-pyridinecarboxylate is used in the synthesis of antitumor agents. Also used in the synthesis of potent CC chemokine receptor 2 antagonists as antiviral and anticancer therapeutics. |
Synthesis route |
Reference: Heterocycles, vol. 39, # 1 p. 163 – 170
Reference: US2009/163472 A1, ; Page/Page column 27 ; US 20090163472 A1
Reference: WO2013/71697 A1, ; Paragraph 00374; |
N-BOC-1,2,3,6-TETRAHYDROPYRIDINE Preparation Products And Raw materials
Upstream information
1-benzylpyridin-1-ium, chloride; 4-Bromotoluene; tert-butyl (3S)-3-methylsulfonyloxypiperidine-1-carboxylate; m-cresol; N-Boc-3-mesyloxypiperidine; tert-butoxycarbonyl anhydride; 4-Hydroxypiperidine; N-Boc-(3-butenyl)(allyl)amine; tert-butyl diallylcarbamate; 1-Benzyl-1, 2, 3, 6-tetrahydropyridine;
Downtream information
1-tert-butyloxycarbonyl-4-(4-methylphenyl)-1, 2, 3, 6-tetrahydropyridine; 4-Fluoropiperidine-N-carboxylic acid tert-butyl ester; N-Boc-1, 2, 3, 6-Tetrahydropyridine;tert-Butyl 7-oxa-3-aza-bicyclo[4. 1. 0]heptane-3-carboxylate; ethene; tert-butyl 4-(4-amino-5-fluoropyrimidin-2-yloxy)piperidine-1-carboxylate; tert-butyl 3-oxo-2, 6-dihydropyridine-1-carboxylate; (RS)-3-(adenin-9-yl)-1-N-tert-butyloxycarbonylpiperidine; (RS)-1-N-tert-butyloxycarbonyl-3-(thymin-1-yl)piperidine; tert-butyl 3-hydroxy-3, 6-dihydro-2H-pyridine-1-carboxylate;
