Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H12ClN.ClH |
Molecular Weight | 170.08 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.ClCCN1CCCC1
InChI
InChIKey=FSNGFFWICFYWQC-UHFFFAOYSA-N
InChI=1S/C6H12ClN.ClH/c7-3-6-8-4-1-2-5-8;/h1-6H2;1H
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C6H12ClN |
Molecular Weight | 133.619 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
1-(2-Chloroethyl)pyrrolidine is a haloalkyl substituted pyrrolidine. It is an intermediate in the synthesis of various pharmaceutical compound. For example, 1-(2-Chloroethyl)pyrrolidine is used for the synthesis of cholinesterase inhibitors and nonsteroidal selective estrogen receptor modulator nafoxidine.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:05:58 GMT 2023
by
admin
on
Sat Dec 16 09:05:58 GMT 2023
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Record UNII |
YYQ1H343R5
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Record Status |
Validated (UNII)
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Record Version |
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