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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
Structure of 1-(2-CHLOROETHYL)PYRROLIDINE HYDROCHLORIDE

SMILES

Cl.ClCCN1CCCC1

InChI

InChIKey=FSNGFFWICFYWQC-UHFFFAOYSA-N
InChI=1S/C6H12ClN.ClH/c7-3-6-8-4-1-2-5-8;/h1-6H2;1H

HIDE SMILES / InChI
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
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

Description

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

Unknown
149124
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Discovery of leukotriene A4 hydrolase inhibitors using metabolomics biased fragment crystallography.
2009-08-13
Patents

Patents

04007272
5
04400543
2
04999362
3
05514675
2
05723492
2
06043269
3
06080754
2
06294532
2
06673803
4
07045528
5
07229987
13
07592358
29
07687643
2
08071586
3
08138199
2
08247430
3
08263772
2
08481536
2
08492560
6
08759517
2

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:29:35 GMT 2025
Edited
by admin
on Mon Mar 31 22:29:35 GMT 2025
Record UNII
YYQ1H343R5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-30132
Preferred Name English
1-(2-CHLOROETHYL)PYRROLIDINE HYDROCHLORIDE
Systematic Name English
N-(2-CHLOROETHYL)PYRROLIDINE HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
NSC
30132
Created by admin on Mon Mar 31 22:29:36 GMT 2025 , Edited by admin on Mon Mar 31 22:29:36 GMT 2025
PRIMARY
CAS
7250-67-1
Created by admin on Mon Mar 31 22:29:36 GMT 2025 , Edited by admin on Mon Mar 31 22:29:36 GMT 2025
PRIMARY
EPA CompTox
DTXSID8022248
Created by admin on Mon Mar 31 22:29:36 GMT 2025 , Edited by admin on Mon Mar 31 22:29:36 GMT 2025
PRIMARY
ECHA (EC/EINECS)
230-660-7
Created by admin on Mon Mar 31 22:29:36 GMT 2025 , Edited by admin on Mon Mar 31 22:29:36 GMT 2025
PRIMARY
FDA UNII
YYQ1H343R5
Created by admin on Mon Mar 31 22:29:36 GMT 2025 , Edited by admin on Mon Mar 31 22:29:36 GMT 2025
PRIMARY
PUBCHEM
81668
Created by admin on Mon Mar 31 22:29:36 GMT 2025 , Edited by admin on Mon Mar 31 22:29:36 GMT 2025
PRIMARY
NIH
NCATS
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