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FENOVERINE

CAS No.
37561-27-6
Chemical Name:
FENOVERINE
Synonyms
FENOVERINE;Spasmopriv;Fenoverine D8;3-chloro-3-oxopropanoic acid ethyl ester;10-[(4-Piperonyl-1-piperazinyl)acetyl]-10H-phenothiazine;Ethanone, 2-[4-(1,3-benzodioxol-5-ylmethyl)-1-piperazinyl]-1-(10H-phenothiazin-10-yl)-
CBNumber:
CB5362347
Molecular Formula:
C26H25N3O3S
Molecular Weight:
459.56
MDL Number:
MFCD00865242
MOL File:
37561-27-6.mol
MSDS File:
SDS
Last updated:2023-05-15 10:43:35

FENOVERINE Properties

Melting point 141-142°
Boiling point 671.8±55.0 °C(Predicted)
Density 1.343±0.06 g/cm3(Predicted)
storage temp. Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility Chloroform (Slightly), Methanol (Slightly)
pka 6.47±0.10(Predicted)
form Solid
color Pale Beige to Beige
Stability Hygroscopic
FDA UNII N274ZQ6PZJ
ATC code A03AX05

SAFETY

Risk and Safety Statements

Toxicity LD50 in mice (g/kg): ~1.50 orally, ~2.50 i.p. (Buzas, Pierre)

FENOVERINE price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC F248898 Fenoverine 37561-27-6 50mg $95 2021-12-16 Buy
TRC F248898 Fenoverine 37561-27-6 250mg $380 2021-12-16 Buy
American Custom Chemicals Corporation API0011437 FENOVERINE 95.00% 37561-27-6 5MG $500.9 2021-12-16 Buy
Medical Isotopes, Inc. 18631 Fenoverine 37561-27-6 5mg $950 2021-12-16 Buy
Product number Packaging Price Buy
F248898 50mg $95 Buy
F248898 250mg $380 Buy
API0011437 5MG $500.9 Buy
18631 5mg $950 Buy

FENOVERINE Chemical Properties,Uses,Production

Originator

Spasmopriv,Paillusseau

Uses

Fenoverine is a colon-specific multi particulate drug. Also, it is an antispasmodic drug which inhibits contraction of smooth muscle. It is derived from Phenothiazine (P318040), which is a key component of antipsychotic and antihistaminic drugs.

Definition

ChEBI: Fenoverine is a member of phenothiazines.

Manufacturing Process

To a hot solution 199.3 g (0.1 mol) of phenothiazine in 2 L of dry benzene was added a little quantity of bromine and then were added dropwise 136 g (0.1 mol) of chloroacetyle chloride. Then a mixture was refluxed for 5 hours. After cooling the mixture was concentrated in vacuo. Product was dissolved at reflux in ethanol absolute and filtered. At room temperature was crystallized chloracetyl-10-phenothiazine with 123°C; yield 242 g.
A mixture of 13.8 g (0.05 mol) of chloracetyl-10-phenothiazine, 11.8 g (0.05 mol) of piperonyl-1-piperazine and 3.9 g (0.05 mol) of pyridine in 200 ml of dry toluene was refluxed for 3 hours. Then the solution was cooled and filtered. The filtrate was concentrated. The crystals of 10-((4-piperonyl-1- piperazinyl)acetyl)phenothiazine was recrystallized from isopropylic ether; M.P. 141-142°C; yield 67%.

Therapeutic Function

Spasmolytic

FENOVERINE Preparation Products And Raw materials

Raw materials

Preparation Products

FENOVERINE Suppliers

Global( 25)Suppliers
Supplier Tel Email Country ProdList Advantage
PT CHEM GROUP LIMITED
+86-85511178 +86-85511178 peter68@ptchemgroup.com China 35453 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58
LGM Pharma 1-(800)-881-8210 inquiries@lgmpharma.com United States 2127 70
TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 24131 58
Cdreamlab (Hubei) Technology Co., LTD 0717-6300888 18062399888 service@cdreamlab.com China 315 58
Cdreamlab (Hubei) Technology Co., LTD 0717-6300888 18062399888 service@cdreamlab.com China 265 58
FENOVERINE 10-[(4-Piperonyl-1-piperazinyl)acetyl]-10H-phenothiazine Spasmopriv 3-chloro-3-oxopropanoic acid ethyl ester Fenoverine D8 Ethanone, 2-[4-(1,3-benzodioxol-5-ylmethyl)-1-piperazinyl]-1-(10H-phenothiazin-10-yl)- 37561-27-6 C26H25N3O3S