Home Categories 1-<WBR>Boc-<WBR>3-<WBR>fluoro-<WBR>4-<WBR>oxopiperidine
A1685112

1-<WBR>Boc-<WBR>3-<WBR>fluoro-<WBR>4-<WBR>oxopiperidine , 95% , 211108-50-8

Synonym(s):
tert-Butyl 3-fluoro-4-oxopiperidine-1-carboxylate;3-Fluoro-4-oxopiperidine-1-carboxylic acid tert-butyl ester

CAS NO.:211108-50-8

Empirical Formula: C10H16FNO3

Molecular Weight: 217.24

MDL number: MFCD10566554

Pack Size Price Stock Quantity
250MG RMB41.60 In Stock
1G RMB94.40 In Stock
5g RMB290.40 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 88-90℃
Boiling point: 288.7±40.0 °C(Predicted)
Density  1.15±0.1 g/cm3(Predicted)
storage temp.  Sealed in dry,Room Temperature
form  powder to crystal
pka -3.61±0.40(Predicted)
color  White to Light yellow
InChI InChI=1S/C10H16FNO3/c1-10(2,3)15-9(14)12-5-4-8(13)7(11)6-12/h7H,4-6H2,1-3H3
InChIKey JZNWQLLPLOQGOI-UHFFFAOYSA-N
SMILES N1(C(OC(C)(C)C)=O)CCC(=O)C(F)C1
CAS DataBase Reference 211108-50-8

Description and Uses

Tert-Butyl 3-Fluoro-4-Oxopiperidine-1-Carboxylate is a versatile compound that finds frequent application in chemical synthesis procedures. This compound serves as a valuable building block due to its unique structural properties and reactivity. Within the realm of organic synthesis, Tert-Butyl 3-Fluoro-4-Oxopiperidine-1-Carboxylate is commonly used as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals.
This compound undergoes a variety of selective reactions, enabling chemists to introduce functional groups at specific positions on the piperidine ring. Its tert-butyl ester group provides steric hindrance, influencing the compound's reactivity and selectivity in subsequent transformations. Additionally, the presence of a fluoro substituent enhances the compound's electronic properties, enabling it to participate in diverse synthetic strategies.Researchers leverage the unique structural features of Tert-Butyl 3-Fluoro-4-Oxopiperidine-1-Carboxylate to access complex molecular architectures efficiently. By incorporating this compound into their synthetic routes, chemists can streamline the synthesis of intricate molecules and accelerate the discovery of novel bioactive compounds. In summary, the versatile nature of Tert-Butyl 3-Fluoro-4-Oxopiperidine-1-Carboxylate makes it an indispensable tool in modern chemical synthesis endeavors.

Safety

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P305+P351+P338
Hazard Codes  Xi
Risk Statements  36-52
WGK Germany  3
HazardClass  IRRITANT
HS Code  2933399990

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