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PHENPROCOUMON

CAS No.
435-97-2
Chemical Name:
PHENPROCOUMON
Synonyms
MARCUMA;Fencumar;Liquamar;Marcumar;Falithrom;Falithiom;Marcoumar;RO 1-4849;Phenprocumon;PHENPROCOUMON
CBNumber:
CB1295890
Molecular Formula:
C18H16O3
Molecular Weight:
280.32
MDL Number:
MFCD00865273
MOL File:
435-97-2.mol
MSDS File:
SDS
Last updated:2023-06-08 09:03:02

PHENPROCOUMON Properties

Melting point 179-180°
Boiling point 463.2±45.0 °C(Predicted)
Density 1.261±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
pka 4.50±1.00(Predicted)
form Solid
color White to Off-White
EWG's Food Scores 1
FDA UNII Q08SIO485D
Proposition 65 List Phenprocoumon
NCI Drug Dictionary Liquamar
ATC code B01AA04
EPA Substance Registry System Phenprocoumon (435-97-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS08,GHS06
Signal word  Danger
Hazard statements  H301-H331-H311-H370
Precautionary statements  P260-P264-P270-P307+P311-P321-P405-P501-P264-P270-P301+P310-P321-P330-P405-P501-P261-P271-P304+P340-P311-P321-P403+P233-P405-P501-P280-P302+P352-P312-P322-P361-P363-P405-P501
RIDADR  2811
HazardClass  6.1(b)
PackingGroup  III
NFPA 704
0
4 0

PHENPROCOUMON price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC P318820 Phenprocoumon 435-97-2 100mg $95 2021-12-16 Buy
Usbiological 165912 Phenprocoumon 435-97-2 1g $460 2021-12-16 Buy
TRC P318820 Phenprocoumon 435-97-2 1g $775 2021-12-16 Buy
TRC P318820 Phenprocoumon 435-97-2 500mg $425 2021-12-16 Buy
American Custom Chemicals Corporation API0003816 PHENPROCOUMON 95.00% 435-97-2 1G $450 2021-12-16 Buy
Product number Packaging Price Buy
P318820 100mg $95 Buy
165912 1g $460 Buy
P318820 1g $775 Buy
P318820 500mg $425 Buy
API0003816 1G $450 Buy

PHENPROCOUMON Chemical Properties,Uses,Production

Chemical Properties

White Solid

Originator

Liquamar ,Organon ,US,1958

Uses

Phenprocoumon is known for being an oral anti-coagulant.

Definition

ChEBI: A hydroxycoumarin that is 4-hydroxycoumarin which is substituted at position 3 by a 1-phenylpropyl group.

Manufacturing Process

8.3 parts by weight of powdered sodium in 300 parts by volume of benzene, 100 parts by weight of diethyl (1'-phenylpropyl)-malonate and 72 parts by weight of acetylsalicylic acid chloride are reacted together to form diethyl 1(o-acetoxybenzoy1)-1-(1'-phenylpropyl)malonate, which boils at 195°198°C/0.03 mm Hg.
10.3 parts of weight of diethyl 1-(o-acetoxybenzoyl)-1-(1'-phenylpropyl)malonate are dissolved in 60 parts by volume of absolute ether and to this solution are added portion. wise at 10°C, while stirring, 2.6 parts by weight of sodium methylate. The reaction mixture is stirred for 4 hours, whereupon it is poured into ice water. The ether solution is washed neutral with ice water. After having distilled off the ether, a thick oil consisting of 3-carbethoxy-3-(1'phenylpropyl)-4-oxo-dihydrocoumarinis obtained. This compound crystallized in butyl oxide and has a MP of 108°-109°C.
The 3-carbethoxy-3-(1'-phenylpropyl)-4-oxo-dihydrocoumarinmay be hydrolyzed and decarboxylated as follows. The crude product is heated to 85°C for 1/2 hour with 100 parts by volume of 5% aqueous sodium hydroxide, while agitating or stirring. To remove traces of undissolved oil, the cooled solution is treated with 1 part by weight of charcoal, whereupon it is filtrated and acidified to Congo reaction with dilute sulfuric acid. The 3-(1'phenylpropyl)-4-hydroxycoumarin formed is separated off and recrystallized in 80% ethanol, whereupon it melts at 178°-179°C according to US Patent 2,701,804.

brand name

Liquamar (Organon).

Therapeutic Function

Anticoagulant

Synthesis

Phenprocoumon, 3-(|á-ethylbenzyl)-4-hydroxycoumarin (24.1.14), is synthesized by acylating sodium salts of diethyl ester (1-phenylpropyl)butyric acid with acetylsalicylic acid chloride, which forms the compound 24.1.12, which upon reaction with sodium ethoxide cyclizes to 3-(|á-ethylbenzyl)-2-carboethoxy-4-hydroxycoumarin (24.1.13). Alkaline hydrolysis of this product and further decarboxylation gives phenprocoumon(24.1.14).

Synthesis_435-97-2

PHENPROCOUMON Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 75)Suppliers
Supplier Tel Email Country ProdList Advantage
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9348 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
Biochempartner
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AFINE CHEMICALS LIMITED
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Dayang Chem (Hangzhou) Co.,Ltd.
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InvivoChem
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TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49999 58
Wuhan Topule Biopharmaceutical Co., Ltd
+8618327326525 masar@topule.com China 8474 58

View Lastest Price from PHENPROCOUMON manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
4-Hydroxy-3-(1-phenylpropyl)-2H-chromen-2-on pictures 2022-02-22 4-Hydroxy-3-(1-phenylpropyl)-2H-chromen-2-on
435-97-2
US $0.00 / KG 1KG 97.4% 100 tons Honest Joy Holdings Limited
PHENPROCOUMON 2H-1-Benzopyran-2-one, 4-hydroxy-3-(1-phenylpropyl)- 3-(1-Phenylpropyl)-4-hydroxycoumarin 3-(1'-Phenyl-propyl)-4-oxycoumarin 3-(alpha-Ethylbenzyl)-4-hydroxycoumarin 4-Hydroxy-3-(1-phenylpropyl)-2H-1-benzopyran-2-one 4-Hydroxy-3-(1-phenylpropyl)-2H-chromen-2-one Coumarin, 3-(alpha-ethylbenzyl)-4-hydroxy- Falithiom Falithrom Fencumar Liquamar Marcoumar Marcumar Phenprocoumarol Phenprocoumarole Phenprocumone RO 1-4849 4-hydroxy-3-(1-phenylpropyl)coumarin PHENYLPROPYL-4-HYDROXYCOUMARIN Phenprocumon 3-(α-Ethylbenzyl)-4-hydroxycoumarin 4-Hydroxy-2-oxo-3-(1-phenylpropyl)-2H-chromene 2-hydroxy-3-[(1S)-1-phenylpropyl]-4H-chroMen-4-one 4-Hydroxy-3-(1-phenylpropyl)-2H-chromen-2-on Phenprocoumon (Marcumar) MARCUMA inhibit,Phenprocoumon,Inhibitor 4-Hydroxy-3-(1-phenyl propyl)-2H-1-Benzopyran Custom 435-97-2