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AE10887

1187932-75-7 | (S)-tert-Butyl 3-(chloromethyl)pyrrolidine-1-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $96.00 $67.00 -   +
500mg 95% in stock $160.00 $112.00 -   +
1g 95% in stock $240.00 $168.00 -   +
5g 95% in stock $758.00 $531.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE10887
Chemical Name: (S)-tert-Butyl 3-(chloromethyl)pyrrolidine-1-carboxylate
CAS Number: 1187932-75-7
Molecular Formula: C10H18ClNO2
Molecular Weight: 219.7084
MDL Number: MFCD08059336
SMILES: ClC[C@H]1CCN(C1)C(=O)OC(C)(C)C

 

Computed Properties
Complexity: 213  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 2  
Rotatable Bond Count: 3  
XLogP3: 2.1  

 

 

Upstream Synthesis Route
  • 1,1-Dimethylethyl (3S)-3-(chloromethyl)-1-pyrrolidinecarboxylate is a versatile compound commonly used in chemical synthesis for a variety of applications. Its primary role lies in the realm of organic chemistry, where it serves as a valuable building block in the creation of complex molecules and pharmaceuticals. This compound's unique structure enables it to participate in a range of important reactions, including nucleophilic substitutions, rearrangements, and reductions. Chemists often utilize 1,1-Dimethylethyl (3S)-3-(chloromethyl)-1-pyrrolidinecarboxylate to introduce specific functional groups or motifs into target molecules, thereby facilitating the synthesis of intricate molecular structures with precision and efficiency. In addition to its synthetic utility, this compound's chirality (specifically the (3S) stereochemistry) allows for the creation of enantiomerically pure products, which is crucial in the pharmaceutical industry and other fields requiring high levels of stereochemical control. Overall, 1,1-Dimethylethyl (3S)-3-(chloromethyl)-1-pyrrolidinecarboxylate plays a crucial role in advancing chemical synthesis by enabling the construction of diverse and complex molecular architectures with strategic control over stereochemistry and functionality.
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