1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde CAS 137076-22-3

Introduction:Basic information about 1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde CAS 137076-22-3, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

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

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)
Fp >110℃
storage temp. 2-8°C
solubility Soluble in methanol.
form Oil
pka-2.13±0.40(Predicted)
color Clear Yellow
Sensitive Air Sensitive
InChIInChI=1S/C11H19NO3/c1-11(2,3)15-10(14)12-6-4-9(8-13)5-7-12/h8-9H,4-7H2,1-3H3
InChIKeyJYUQEWCJWDGCRX-UHFFFAOYSA-N
SMILESN1(C(OC(C)(C)C)=O)CCC(C=O)CC1
CAS DataBase Reference137076-22-3(CAS DataBase Reference)

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
WGK Germany WGK 3
HS Code 29333990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3

1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde Usage And Synthesis

Chemical PropertiesClear Yellow Oil
UsesReactant 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
Uses1-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
UsesAn intermediate for polycyclic indazole derivatives that are ERK inhibitors.

1-tert-Butoxycarbonyl-4-piperidinecarboxaldehyde Preparation Products And Raw materials

Raw materialsDichloromethane-->Lithium Aluminum Hydride-->Di-tert-butyl dicarbonate-->Sodium acetate-->Manganese dioxide-->Pyridinium chlorochromate-->Isonipecotic acid-->4-Piperidinemethanol
Preparation Productstert-butyl 2-oxo-8-azaspiro[4.5]decane-8-carboxylate-->tert-butyl 4-(1H-benzo[d]iMidazol-2-yl)piperidine-1-carboxylate-->1-BOC-PIPERIDIN-4-YLPROPIONIC ACID-->TERT-BUTYL 9-OXO-3-AZASPIRO[5.5]UNDECANE-3-CARBOXYLATE-->1-Boc-4-(2-aMino-1-hydroxybutyl)piperidine-->tert-butyl 4-(2-fluoro-3-hydroxypropyl)piperidine-1-carboxylate-->1-Boc-4-(1-phenylacetoxyallyl)piperidine-->CHEMBRDG-BB 4005904
1-PYREN-4-YL-ETHANONE CAS 22245-47-2
1-Triacontanol CAS 593-50-0
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