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Merck
CN

139521

2-(2-Chloroethyl)-1-methylpyrrolidine hydrochloride

99%

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About This Item

Empirical Formula (Hill Notation):
C7H14ClN · HCl
CAS Number:
Molecular Weight:
184.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
260-395-2
Beilstein/REAXYS Number:
6148386
MDL number:
Assay:
99%
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Quality Level

assay

99%

mp

98-102 °C (lit.)

functional group

chloro

SMILES string

Cl[H].CN1CCCC1CCCl

InChI

1S/C7H14ClN.ClH/c1-9-6-2-3-7(9)4-5-8;/h7H,2-6H2,1H3;1H

InChI key

KCQMALZNENFGKK-UHFFFAOYSA-N

Application

2-(2-Chloroethyl)-1-methylpyrrolidine hydrochloride was used in the synthesis of N-[2-(1-methylpyrrolidin-2-yl)ethyl]-N-(2-iodo-4,5-dimethoxyphenyl) amide. It was used as reagent during the synthesis of 1-methyl-2-[2-[2-(2-phenylethyl)phenoxy]ethyl]pyrrolidine hydrochlochloride.


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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N Tanaka et al.
Chemical & pharmaceutical bulletin, 48(2), 245-255 (2000-03-08)
A series of [2-(omega-phenylalkyl)phenoxy]alkylamines was synthesized and their receptor binding affinity was examined in vitro. These compounds showed an affinity for serotonin-2 (5-HT2) and dopamine-2 (D2) receptors. [2-(2-phenylethyl)phenoxy]alkylamine derivatives with a pyrrolidine or piperidine moiety in the structure showed higher
Shejin Zhu et al.
Bioorganic & medicinal chemistry, 14(9), 3131-3143 (2006-01-18)
6-Substituted 8,9-dimethoxy-2,3-methylenedioxy-6H-dibenzo[c,h][2,6]naphthyridin-5-ones were synthesized and evaluated for topoisomerase I-targeting activity and cytotoxicity. Several of these reversed lactam analogues of ARC-111 exhibited exceptional cytotoxicity with IC50 values ranging from 0.5 to 3.0 nM. In contrast to topotecan, no resistance was observed



Global Trade Item Number

SKUGTIN
139521-5G04061838732880
139521-25G04061832241852