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Afloqualone

CAS No.
56287-74-2
Chemical Name:
Afloqualone
Synonyms
H-495;aroft;HQ-495;HQ 495;arofuto;Aoqualone;AFLOQUALONE;Afloquanone;Afloqualone D7;Afloqualone USP/EP/BP
CBNumber:
CB3699964
Molecular Formula:
C16H14FN3O
Molecular Weight:
283.3
MDL Number:
MFCD00867693
MOL File:
56287-74-2.mol
Last updated:2023-07-07 16:22:03

Afloqualone Properties

Melting point 195-196°C
Boiling point 492.5±55.0 °C(Predicted)
Density 1.2529 (estimate)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka 2.73±0.70(Predicted)
color White to Off-White
InChI InChI=1S/C16H14FN3O/c1-10-4-2-3-5-14(10)20-15(9-17)19-13-7-6-11(18)8-12(13)16(20)21/h2-8H,9,18H2,1H3
InChIKey VDOSWXIDETXFET-UHFFFAOYSA-N
SMILES N1C2=C(C=C(N)C=C2)C(=O)N(C2=CC=CC=C2C)C=1CF
CAS DataBase Reference 56287-74-2(CAS DataBase Reference)
FDA UNII CO4U2C8ORZ

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Toxicity LD50 in mice (mg/kg): 315.1 i.p. (Tani)
NFPA 704
0
2 0

Afloqualone price More Price(18)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 21834 Afloqualone ≥98% 56287-74-2 1mg $81 2024-03-01 Buy
Cayman Chemical 21834 Afloqualone ≥98% 56287-74-2 5mg $355 2024-03-01 Buy
TRC A357700 Afloqualone 56287-74-2 1g $300 2021-12-16 Buy
Matrix Scientific 143959 6-Amino-2-(fluoromethyl)-3-(o-tolyl)quinazolin-4(3H)-one 95% 56287-74-2 1g $800 2021-12-16 Buy
Matrix Scientific 143959 6-Amino-2-(fluoromethyl)-3-(o-tolyl)quinazolin-4(3H)-one 95% 56287-74-2 5g $2332 2021-12-16 Buy
Product number Packaging Price Buy
21834 1mg $81 Buy
21834 5mg $355 Buy
A357700 1g $300 Buy
143959 1g $800 Buy
143959 5g $2332 Buy

Afloqualone Chemical Properties,Uses,Production

Description

Afloqualone is a centrally acting muscle relaxant useful in the management of various spastic conditions, including cerebral palsy, cervical spondylosis, and multiple sclerosis. It is closely related to the hypnotidsedative methaqualone.

Description

Afloqualone (Item No. 21834) is an analytical reference standard categorized as a quinazolinone. This product is intended for research and forensic applications.

Originator

Tanabe (Japan)

Uses

Afloqualone acts as a muscle relaxant in humans and may be used in the treatment of muscle spasms affecting rheumatoid arthritis.

Definition

ChEBI: Afloqualone is an organic molecular entity.

Manufacturing Process

14.4 g (0.053 mol) of N-(2-amino-5-nitrobenzoyl)-o-toluidine and 6.3 g (0.08 mol) of pyridine are dissolved in 300 ml of tetrahydrofuran. 12.2 g (0.126 mol) of fluoroacetyl chloride are added to the solution for 10 minutes under ice-cooling. The solution is stirred at the same temperature for 30 minutes and then at room temperature for 2.5 hours. The reaction solution is allowed to stand at room temperature overnight. The crystalline precipitate is collected by filtration, washed with water and then dried. 16.4 g of N-(2- fluoroacetamido-5-nitrobenzoyl)-o-toluidine are obtained. Yield: 93.7%; MP 238-239°C.
16.5 g (0.05 mol) of N-(2-fluoroacetamido-5-nitrobenzoyl)-o-toluidine and 25.5 g (0.25 mol) of acetic acid anhydride are dissolved in 250 ml of glacial acetic acid. The solution is refluxed for 2 hours under heating. Then, the reaction solution is evaporated to remove solvent. The residue thus obtained is poured into ice-water, and the aqueous mixture is adjusted to pH 9 with potassium carbonate. The crystalline precipitate is collected by filtration. 15.5 g of 2-fluoromethyl-3-(o-tolyl)-6-nitro-4(3H)-quinazolinone are obtained. Yield: 98.7%; MP 155-158°C (recrystallized from ethanol).
A mixture of 2.0 g (0.064 mol) of 2-fluoromethyl-3-(o-tolyl)-6-nitro-4(3H)- quinazolinone, 0.2 g of 5% palladium-carbon and 100 ml of acetic acid is shaken for 30 minutes in hydrogen gas. The initial pressure of hydrogen gas is adjusted to 46 lb and the mixture is heated with an infrared lamp during the reaction. After 30 minutes of this reaction, the pressure of hydrogen gas decreases to 6 lb. After the mixture is cooled, the mixture is filtered to remove the catalyst. The filtrate is evaporated to remove acetic acid, and the residue is dissolved in chloroform. The chloroform solution is washed with 5% aqueous sodium hydroxide and water, successively. Then, the solution is dried and evaporated to remove solvent. The oily residue thus obtained is dissolved in 2 ml of chloroform, and the chloroform solution is passed through a column of 200 g of silica gel. The silica gel column is eluted with ethyl acetatebenzene (1:1). Then, the eluate is evaporated to remove solvent. The crude crystal obtained is washed with isopropyl ether and recrystallized from isopropanol. 0.95 g of 2-fluoromethyl-3-(o-tolyl)-6-amino-4(3H)-quinazolinone is obtained. Yield: 52.5%; MP 195-196°C.

brand name

AROFUTO

Therapeutic Function

Muscle relaxant

Afloqualone Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 141)Suppliers
Supplier Tel Email Country ProdList Advantage
Shanghai Jinhuan Chemical CO.,LTD.
+86-21-52210535 +8613162045318 sales@jinhchem.com China 332 58
Shanghai Time Chemicals CO., Ltd.
+86-021-57951555 +8617317452075 jack.li@time-chemicals.com China 1807 55
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Xiamen AmoyChem Co., Ltd
+86-592-6051114 +8618959220845 sales@amoychem.com China 6387 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
Fuxin Pharmaceutical
+86-021-021-50872116 +8613122107989 contact@fuxinpharm.com China 10297 58
SIMAGCHEM CORP
+86-13806087780 sale@simagchem.com China 17367 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671 sales@tnjchem.com China 34572 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29271 58

View Lastest Price from Afloqualone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Afloqualone USP/EP/BP pictures 2021-07-08 Afloqualone USP/EP/BP
56287-74-2
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited
Afloqualone pictures 2019-07-06 Afloqualone
56287-74-2
US $1.00 / kg 1kg 99% 100KG Career Henan Chemical Co
  • Afloqualone pictures
  • Afloqualone
    56287-74-2
  • US $1.00 / kg
  • 99%
  • Career Henan Chemical Co
Afloqualone 6-Amino-2-(fluoromethyl)-3-(2-methylphenyl)-quinazolin-4-one 6-Amino-2-fluoromethyl-3-(o-tolyl)-quinazolin-4(3H)-one H-495 HQ 495 HQ-495 Afloquanone 6-aMino-2-fluoroMethyl-3-(o-tolyl)-4(3h)-quinaz... 6-amino-2-(fluoromethyl)-3-(2-methylphenyl)-4(3h)-quinazolinon 6-amino-2-fluoromethyl-3-(o-tolyl)-4(3h)-quinazolinon 6-amino-2-(fluoromethyl)-3-(2-methylphenyl)-quinazolin-4-one AFLOQUALONE 6-amino-2-fluoromethyl-3-(o-tolyl)-4(3h)-quinazolinone aroft arofuto 6-Amino-2-Fluoromethyl-3-(2-Tolyl)-3H-quinazolin-4-one 4(3H)-Quinazolinone, 6-amino-2-(fluoromethyl)-3-(2-methylphenyl)- 6-amino-2-(fluoromethyl)-3-(2-methylphenyl)quinazolin-4(3H)-one 6-amino-2-(fluoromethyl)-3-(2-methylphenyl)-4-quinazolinone Aoqualone Afloqualone USP/EP/BP Afloqualone D7 Dibenzofuran Impurity 2 56287-74-2 6287-74-2 API Other APIs