carfenazine hydrogen maleate

Product Name
carfenazine hydrogen maleate
CAS No.
2975-34-0
Chemical Name
carfenazine hydrogen maleate
Synonyms
Wy 2445;NSC71755;Aids031736;Aids-031736;Proketazine;Carphenazin Maleate;Carfenazine Maleate;Proketazine maleate;Proketazine dimaleate;Carphenazine dimaleate
CBNumber
CB9876750
Molecular Formula
C28H35N3O6S
Formula Weight
541.659
MOL File
2975-34-0.mol
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carfenazine hydrogen maleate Property

Melting point:
175-177° (Tislow); mp 165-167° (Sherlock, Sperber)
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
color 
Yellow
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
C184300
Product name
CarphenazineDimaleate
Packaging
5mg
Price
$140
Updated
2021/12/16
TRC
Product number
C184300
Product name
CarphenazineDimaleate
Packaging
50mg
Price
$1110
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0009303
Product name
CARPHENAZINE MALEATE
Purity
95.00%
Packaging
500MG
Price
$1871.1
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC19823
Product name
Carphenazine dimaleate
Packaging
10mg
Price
$110
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC19823
Product name
Carphenazine dimaleate
Packaging
25mg
Price
$205
Updated
2021/12/16
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carfenazine hydrogen maleate Chemical Properties,Usage,Production

Originator

Proketazine,Wyeth,US,1962

Uses

Antipsychotic.

Definition

ChEBI: A maleate salt derived from carphenazine.

Manufacturing Process

As described in US Patent 3,023,146, in a round-bottomed flask were placed 35 g of 2-propionyl phenothiazine (0.14 mol) 7 g of 50% sodium hydride in mineral oil (0.14 mol), and 240 cc of dimethyl formamide dried over sodium hydride. The resultant solution was stirred at room temperature for 2 hours, and then 88 g (0.56 mol) of trimethylene chlorobromide was added at once.
The mixture was stirred for 2 hours, heated at 60 to 70°C for 1 hour and poured into 2 liters of H2O. The resulting suspension was extracted with ether, the ether layer separated and the ether removed under vacuum. A gummy mass remained which was dissolved in decalin and the solution was partly distilled to remove excess chlorobromide. After removal of most of the decalin under vacuum, the residue was treated with a large excess of N-(β- hydroxyethyl)-piperazine and heated on a steam bath for 2 hours. This material was extracted with dilute aqueous HCl, this acid layer neutralized with aqueous base and the resulting oil extracted into ether. The ether layer was washed with water until the washings were neutral and dried over anhydrous potassium carbonate. On treatment with maleic acid in ether a yellow solid separated which was recrystallized from isopropanol. This yellow solid had MP 175° to 177°C.

brand name

Proketazine (Wyeth).

Therapeutic Function

Tranquilizer

carfenazine hydrogen maleate Preparation Products And Raw materials

Raw materials

Preparation Products

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carfenazine hydrogen maleate Suppliers

Carbosynth
Tel
--
Fax
--
Email
sales@carbosynth.com
Country
United Kingdom
ProdList
6005
Advantage
58

2975-34-0, carfenazine hydrogen maleate Related Search:


  • carfenazine hydrogen maleate
  • NSC71755
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  • Aids031736
  • Aids-031736
  • Carphenazine dimaleate
  • Proketazine maleate
  • 1-[10-[3-[4-(2-Hydroxyethyl)-1-piperazinyl]propyl]-10H-phenothiazin-2-yl]-1-propanone (2Z)-2-Butenedioate
  • Carfenazine Maleate
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  • Wy 2445
  • Procethazine dimaleate
  • Proketazine
  • Proketazine dimaleate
  • 2975-34-0
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  • Amines, Aromatics, Heterocycles, Pharmaceuticals, Intermediates & Fine Chemicals, Sulfur & Selenium Compounds
  • Amines
  • Aromatics
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Sulfur & Selenium Compounds