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Clortermine

CAS No.
10389-72-7
Chemical Name:
Clortermine
Synonyms
SU-10568;Su 10568;Clortermine;Clortermine HCl;UNII-33L9ZA65K4;Clortermine hydrochloride;o-Chloro-a,a-dimethylphenethylamine Hydrochloride;o-Chloro-α,α-dimethylphenethylamine Hydrochloride
CBNumber:
CB01178364
Molecular Formula:
C10H14ClN*ClH
Molecular Weight:
220.14
MDL Number:
MFCD01708325
MOL File:
10389-72-7.mol
Last updated:2023-05-29 13:57:48

Clortermine Properties

Melting point 245-246°
FDA UNII 33L9ZA65K4

SAFETY

Risk and Safety Statements

Toxicity LD50 orally in rats: 332 ±23 mg/kg (Goldenthal)
DEA Controlled Substances CSCN: 1647
CAS SCH: III
NARC: N

Clortermine price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC C428653 o-Chloro-α,α-dimethylphenethylamineHydrochloride 10389-72-7 250mg $340 2021-12-16 Buy
American Custom Chemicals Corporation HCH0071431 1-(2-CHLOROPHENYL)-2-METHYLPROPAN-2-AMINE HYDROCHLORIDE 95.00% 10389-72-7 1G $925.31 2021-12-16 Buy
American Custom Chemicals Corporation HCH0071431 1-(2-CHLOROPHENYL)-2-METHYLPROPAN-2-AMINE HYDROCHLORIDE 95.00% 10389-72-7 2.5G $1363.65 2021-12-16 Buy
American Custom Chemicals Corporation HCH0071431 1-(2-CHLOROPHENYL)-2-METHYLPROPAN-2-AMINE HYDROCHLORIDE 95.00% 10389-72-7 5G $1759.28 2021-12-16 Buy
Product number Packaging Price Buy
C428653 250mg $340 Buy
HCH0071431 1G $925.31 Buy
HCH0071431 2.5G $1363.65 Buy
HCH0071431 5G $1759.28 Buy

Clortermine Chemical Properties,Uses,Production

Originator

Voranil,U.S.V.,US,1973

Uses

o-Chloro-α,α-dimethylphenethylamine Hydrochloride is derived from 4-Chloro-N-(2-chloropropyl)benzeneethanamine Hydrochloride (C364255), which is used as a reagent in the synthesis of Lorcaserin (L469890, HCl); a novel selective 5-HT2C-receptor agonist for the treatment of obesity.

Uses

Anorexic.

Manufacturing Process

To a Grignard reagent (prepared from 50.0 g of o,α-dichloro-toluene and 7.45 g of magnesium in diethyl ether) is added 18.0 g of acetone at such rate that constant reflux is maintained. The reaction mixture is allowed to stand overnight at room temperature, and is then poured onto a mixture of 20% sulfuric acid and ice. The organic layer is separated, washed with water, an aqueous solution of sodium hydrogen carbonate and again with water, dried over magnesium sulfate and evaporated to dryness. The residue is distilled under reduced pressure to yield 42.6 g of 1-(o-chlorophenyl)-2-methyl-2- propanol, BP 120° to 122°C/12.5 mm.
To 29.0 ml of glacial acetic acid, cooled to 15°C, is added 11.5 g of sodium cyanide (98%) while stirring, and then dropwise 32.4 ml of concentrated sulfuric acid, dissolved in 29 ml of glacial acetic acid, while maintaining a temperature of 20°C. The 1-(o-chlorophenyl)-2-methyl-2-propanol is added moderately fast, allowing the temperature to rise spontaneously. After completing the addition, the reaction mixture is heated to 70°C and stirred, and is then poured onto a mixture of water and ice. The aqueous mixture is neutralized with sodium carbonate and extracted with diethyl ether. The organic solution is washed with water, dried over magnesium sulfate and evaporated to dryness.
The oily residue is taken up in 100 ml of 6 N aqueous hydrochloric acid and refluxed until a clear solution is obtained. The latter is made basic with aqueous ammonia and extracted with diethyl ether; the organic solution is separated, washed, dried and evaporated. The residue is distilled under reduced pressure to yield 26.3 g of 1-(o-chlorophenyl)-2-methyl-2- propylamine, BP 116° to 118°C/16 mm.
The 1-(o-chlorophenyl)-2-methyl-2-propylamine hydrochloride is prepared by adding ethanolic hydrogen chloride to an ice-cold solution of the free base in ethanol; the desired salt precipitates and is recrystallized from ethanol, MP 245° to 246°C.

Therapeutic Function

Antiobesity

Clortermine Preparation Products And Raw materials

Raw materials

Preparation Products

Clortermine Suppliers

Global( 5)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
Supplier Advantage
TargetMol Chemicals Inc.
58
Clortermine Clortermine hydrochloride o-Chloro-α,α-dimethylphenethylamine Hydrochloride o-Chloro-a,a-dimethylphenethylamine Hydrochloride Clortermine HCl Su 10568 SU-10568 UNII-33L9ZA65K4 10389-72-7