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Noxiptiline

Product Name
Noxiptiline
CAS No.
3362-45-6
Chemical Name
Noxiptiline
Synonyms
Sipcar;Dibenzoxin;noxiptilin;Noxiptyline;Noxiptiline;10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-one O-[2-(dimethylamino)ethyl]oxime;5H-Dibenzo[a,d]cyclohepten-5-one, 10,11-dihydro-, O-[2-(dimethylamino)ethyl]oxime
CBNumber
CB21179365
Molecular Formula
C19H22N2O
Formula Weight
294.39
MOL File
3362-45-6.mol
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Noxiptiline Property

Boiling point:
bp0.05 160-164°
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0012099
Product name
NOXIPTILINE
Purity
95.00%
Packaging
5MG
Price
$497.26
Updated
2021/12/16
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Noxiptiline Chemical Properties,Usage,Production

Originator

Agedal,Bayer,W. Germany ,1969

Definition

ChEBI: Noxiptiline is an organic tricyclic compound.

Manufacturing Process

15 grams 5-keto-10,11-dihydrodibenzo-[a,d]cycloheptene dissolved in 225 ml of pyridine was mixed with 15 grams hydroxylamine hydrochloride, and the mixture was boiled under reflux for 22 hours. The bulk of the pyridine was then distilled off under reduced pressure, the residue was poured into water, and the aqueous mixture thus formed was extracted with ether.
The ether extract was washed with water, dried and heated to distill off the ether. The solid residue was recrystallized from a mixture of benzene and light petroleum (BP 40° to 60°C). 12.8 grams of the recrystallized oxime had a MP of 167° to 169°C.
A solution of 22 grams of the above described 5-oximino-10,11dihydrodibenzo-[a,d]cycloheptene in 120 ml benzene was treated with 7.8grams sodamide and the mixture was stirred and heated under reflux for 2 hours. At this stage, the 14.4 grams of hydrochloride of β-(dimethylamino) ethyl chloride was added and heating under reflux was continued for 16 hours. 50 ml water was then cautiously added to decompose unreacted sodamide and the benzene layer was separated and extracted with dilute (10%) aqueous hydrochloric acid.
The aqueous acid extracts were made alkaline with concentrated aqueous potassium hydroxide solution and then extracted with ether. The ether extracts were dried, the solvent was removed and the residual oil was distilled under reduced pressure. The product was 14.5 grams of the fraction boiling at 160° to 164°C, under a pressure of 0.05 mm of mercury.

Therapeutic Function

Psychostimulant

Noxiptiline Preparation Products And Raw materials

Raw materials

Preparation Products

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Noxiptiline Suppliers

Career Henan Chemica Co
Tel
+86-0371-86658258 +8613203830695
Fax
0371-86658258
Email
laboratory@coreychem.com
Country
China
ProdList
30240
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58
Nanjing Finetech Chemical Co., Ltd.
Tel
025-85710122 17714198479
Fax
025-85710122
Email
sales@fine-chemtech.com
Country
CHINA
ProdList
885
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55
Shaanxi Didu New Materials Co. Ltd
Tel
+86-89586680 +86-13289823923
Email
1026@dideu.com
Country
China
ProdList
8670
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58
Lanospharma Laboratories Co.,Ltd
Tel
--
Fax
--
Email
sales@lanospharma.com
Country
China
ProdList
6329
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56
Shanghai New Union Textra Import & Export Co., Ltd
Tel
--
Fax
--
Email
zhou@pharmchemical.com
Country
China
ProdList
2748
Advantage
60

3362-45-6, NoxiptilineRelated Search:


  • Noxiptiline
  • noxiptilin
  • 10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-one O-[2-(dimethylamino)ethyl]oxime
  • Dibenzoxin
  • Noxiptyline
  • Sipcar
  • 5H-Dibenzo[a,d]cyclohepten-5-one, 10,11-dihydro-, O-[2-(dimethylamino)ethyl]oxime
  • 3362-45-6