cycrimine hydrochloride

Product Name
cycrimine hydrochloride
CAS No.
126-02-3
Chemical Name
cycrimine hydrochloride
Synonyms
NSC 169452;CoMpound 8958;Pagitane hydrochloride;cycrimine hydrochloride;Benzhexol Impurity 14(Cycrimine Hydrochloride);1-cyclopentyl-1-phenyl-3-piperidino-propan-1-ol hydrochloride;1-cyclopentyl-1-phenyl-3-piperidin-1-ylpropan-1-ol hydrochloride;1-cyclopentyl-1-phenyl-3-piperidin-1-yl-propan-1-ol hydrochloride;1-Piperidinepropanol, .alpha.-cyclopentyl-.alpha.-phenyl-, hydrochloride
CBNumber
CB1904475
Molecular Formula
C19H29NO.ClH
Formula Weight
0
MOL File
126-02-3.mol
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cycrimine hydrochloride Property

Melting point:
239 - 241°C
storage temp. 
-20°C Freezer, Under inert atmosphere
solubility 
DMSO (Slightly, Heated), Methanol (Slightly), Water (Slightly)
form 
Solid
color 
White
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
C991450
Product name
CycrimineHydrochloride
Packaging
50mg
Price
$145
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0002162
Product name
CYCRIMINE HYDROCHLORIDE
Purity
95.00%
Packaging
5MG
Price
$499.55
Updated
2021/12/16
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cycrimine hydrochloride Chemical Properties,Usage,Production

Originator

Pagitane,Lilly,US,1953

Uses

Cycrimine Hydrochloride is a cholinolytic anti-Parkinson drug which can cause neuromuscular blockades in isolated rat diaphragms.

Definition

ChEBI: The hydrochloride salt of cycrimine. A central anticholinergic, it is used as its hydrochloride salt in the management and treatment of Parkinson's disease.

Manufacturing Process

The manufacture of the cyclohexyl analog is as follows. Phenyl magnesium bromide was prepared from 48.5 g (0.308 mol) of bromobenzene, 7 g (0.29 mol) of magnesium, and 125 ml of dry ether. To it was added at 5°C over a period of ? hour 40 g (0.18 mol) of cyclohexyl β-(N-piperidyl)-ethyl ketone (BP 115° to 117°C/1 mm) in 125 ml of dry ether. The mixture was allowed slowly to come to room temperature, refluxed for one hour, and then poured into ice containing 80 ml of concentrated hydrochloric acid. Ammonium chloride (100 g) and 200 ml of concentrated ammonium hydroxide were added and the organic layer was separated. After drying and removing the solvent, the residue was distilled under reduced pressure. The base distilled at 158° to 170°C (1 mm) and solidified. Upon recrystallization from methanol it melted at 112° to 113°C.

brand name

Pagitane (Lilly).

Therapeutic Function

Muscle relaxant, Antiparkinsonian

cycrimine hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

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cycrimine hydrochloride Suppliers

Alfa Chemistry
Tel
+1-5166625404
Fax
1-516-927-0118
Email
Info@alfa-chemistry.com
Country
United States
ProdList
21317
Advantage
58
Energy Chemical
Tel
021-58432009 400-005-6266
Fax
021-58436166
Email
marketing1@energy-chemical.com
Country
China
ProdList
44894
Advantage
58
Guangzhou Juntang Technology Co., Ltd
Tel
020-36607679 13502246435
Email
sales@dmstandards.com
Country
China
ProdList
10951
Advantage
58
Shaanxi Dideu Medichem Co. Ltd
Tel
029-81124267 15229202216
Fax
029-88380327
Email
1073@dideu.com
Country
China
ProdList
10011
Advantage
58
LGC Science (Shanghai) Ltd.
Tel
17717235263
Email
cindy.yang@lgcgroup.com
Country
China
ProdList
11572
Advantage
58
China National Standard Pharmaceutical Corporation Limited
Tel
+8615391658522
Email
overseasales@yongstandards.com
Country
China
ProdList
11927
Advantage
58
Hangzhou MolCore BioPharmatech Co.,Ltd.
Tel
+86-057181025280; +8617767106207
Fax
0571-85806285
Email
sales@molcore.com
Country
China
ProdList
49739
Advantage
58

126-02-3, cycrimine hydrochlorideRelated Search:


  • cycrimine hydrochloride
  • 1-Piperidinepropanol, .alpha.-cyclopentyl-.alpha.-phenyl-, hydrochloride
  • 1-cyclopentyl-1-phenyl-3-piperidin-1-yl-propan-1-ol hydrochloride
  • 1-cyclopentyl-1-phenyl-3-piperidin-1-ylpropan-1-ol hydrochloride
  • 1-cyclopentyl-1-phenyl-3-piperidino-propan-1-ol hydrochloride
  • CoMpound 8958
  • NSC 169452
  • Pagitane hydrochloride
  • Benzhexol Impurity 14(Cycrimine Hydrochloride)
  • 126-02-3