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tolciclate

CAS No.
50838-36-3
Chemical Name:
tolciclate
Synonyms
K 9147;KC 9147;Fungifos;Tolmicen;Kilmicen;Aids029681;Aids-029681;1,4-Methanonaphthalene, carbamothioic acid deriv.;N-Methyl-N-(m-tolyl)thiocarbamic acid O-(1,2,3,4-tetrahydro-1,4-methanonaphthalen-6-yl) ester;N-(3-Methylphenyl)-N-methylthiocarbamic acid O-(1,2,3,4-tetrahydro-1,4-methanonaphthalen-6-yl) ester
CBNumber:
CB7893256
Molecular Formula:
C20H21NOS
Molecular Weight:
323.45
MDL Number:
MFCD01739034
MOL File:
50838-36-3.mol
Last updated:2024-03-16 15:43:42

tolciclate Properties

Melting point 92-94°
Boiling point 447.3±55.0 °C(Predicted)
Density 1.0965 (rough estimate)
refractive index 1.5800 (estimate)
pka -0.42±0.50(Predicted)
FDA UNII T3TZ02X2AZ

SAFETY

Risk and Safety Statements

Toxicity LD50 in mice, rats, dogs (mg/kg): 4000, 6000, 5000 orally (deCarneri)

tolciclate price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0004442 TOLCICLATE 95.00% 50838-36-3 5MG $496.07 2021-12-16 Buy
Product number Packaging Price Buy
API0004442 5MG $496.07 Buy

tolciclate Chemical Properties,Uses,Production

Originator

Tolmicen,Carlo Erba,Italy,1979

Definition

ChEBI: Tolciclate is a monothiocarbamic ester. It has a role as an antifungal drug.

Indications

The indications for tolciclate are defined by its narrow spectrum and limited to the treatment of dermatophytoses. Because of inadequate penetration into the nail keratin, it is unlikely to be effective for the treatment of onychomycoses. On average, the efficacy of tolciclate in topical therapy of dermatomycoses is lower than that of most other antimycotics for topical treatment.

Manufacturing Process

Thiophosgene (1.15 g, 0.01 mol) in chloroform (40 ml) was slowly treated at room temperature with sodium 1,4-methano-1,2,3,4-tetrahydro-6- naphthoxide (1.82 g, 0.01 mol). After 30 minutes, N-methyl-m-toluidine (2.42 g, 0.02 mol) in chloroform (40 ml) was added dropwise to the solution so obtained at room temperature. The reaction mixture was stirred for 48 hours at room temperature and then refluxed for 2 hours. The solvent was evaporated, and the residue redissolved in water and extracted repeatedly with diethyl ether. The organic phase was dried (Na2SO4) and evaporated to dryness to give, after crystallization from isopropanol, O-(1,4-methano- 1,2,3,4-tetrahydro-6-naphthyl)-N-methyl-N-(m-tolyl)-thiocarbamate (1.3 g) melting point 92°C to 94°C.

Therapeutic Function

Topical antimycotic

Antimicrobial activity

In vitro, tolciclate has a narrow activity spectrum with good efficacy only towards dermatophytes. Isolates of susceptible species showing primary resistance or developing secondary resistance are rarely observed.

463-71-8
50838-54-5
696-44-6
50838-36-3
Synthesis of tolciclate from Thiophosgene and 1,4-Methanonaphthalen-6-ol, 1,2,3,4-tetrahydro- and 3-(Methylamino)toluene

tolciclate Preparation Products And Raw materials

Raw materials

Preparation Products

tolciclate Suppliers

Global( 5)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Hangzhou MolCore BioPharmatech Co.,Ltd.
+86-057181025280; +8617767106207 sales@molcore.com China 49739 58
TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 24131 58

50838-36-3(tolciclate)Related Search:

1,4-Methanonaphthalene, carbamothioic acid deriv. Carbamothioic acid, methyl(3-methylphenyl)-, O-(1,2,3,4-tetrahydro-1,4-methanonaphthalen-6-yl) ester (9CI) Fungifos K 9147 KC 9147 Kilmicen Tolmicen N-(3-Methylphenyl)-N-methylthiocarbamic acid O-(1,2,3,4-tetrahydro-1,4-methanonaphthalen-6-yl) ester N-(3-Methylphenyl)-N-methylthiocarbamic acid O-(1,2,3,4-tetrahydro-1,4-methanonaphthalenanonaphthalen-6-yl) N-Methyl-N-(m-tolyl)thiocarbamic acid O-(1,2,3,4-tetrahydro-1,4-methanonaphthalen-6-yl) ester Aids029681 Aids-029681 Carbamothioic acid, methyl(3-methylphenyl)-, o-(1,2,3,4-tetrahydro-1,4-methanonaphthalen-6-yl) ester Carbamothioic acid, N-methyl-N-(3-methylphenyl)-, O-(1,2,3,4-tetrahydro-1,4-methanonaphthalen-6-yl) ester 50838-36-3