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(2-HYDROXY-2-PHENYL-ETHYL)-METHYL-CARBAMIC ACID TERT-BUTYL ESTER, also known as tioconazole, is a synthetic antifungal medication with potent inhibitory effects on the growth of fungi, particularly Candida species, which are the primary causative agents of vaginal yeast infections.
Used in Pharmaceutical Industry:
(2-HYDROXY-2-PHENYL-ETHYL)-METHYL-CARBAMIC ACID TERT-BUTYL ESTER is used as an antifungal agent for the treatment of vaginal yeast infections. It effectively targets and inhibits the growth of Candida species, providing relief from the discomfort and itching associated with these infections.
Used in Medicinal Formulations:
(2-HYDROXY-2-PHENYL-ETHYL)-METHYL-CARBAMIC ACID TERT-BUTYL ESTER is used as an active ingredient in various medicinal formulations such as creams, ointments, and suppositories for vaginal administration. These formulations facilitate targeted treatment and ensure effective delivery of the medication to the site of infection.
Used in Allergy Management:
(2-HYDROXY-2-PHENYL-ETHYL)-METHYL-CARBAMIC ACID TERT-BUTYL ESTER is used as a component in allergy management, as individuals with known allergies to tioconazole or related compounds should avoid using this medication to prevent adverse reactions.

77184-09-9

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77184-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77184-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,8 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77184-09:
(7*7)+(6*7)+(5*1)+(4*8)+(3*4)+(2*0)+(1*9)=149
149 % 10 = 9
So 77184-09-9 is a valid CAS Registry Number.

77184-09-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(β-Hydroxyphenaethyl)-N-methyl-carbaminsaeure-(t-butyl)ester

1.2 Other means of identification

Product number -
Other names tert-Butyl (2-hydroxy-2-phenylethyl)(methyl)carbamate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:77184-09-9 SDS

77184-09-9Relevant academic research and scientific papers

NEW COMPOUNDS MODULATING GAMMA-SECRETASE AND THEIR USE IN THE TREATMENT OF ALPHA BETA RELATED PATHOLOGIES, SUCH AS ALZHEIMER'S DISEASE

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Page/Page column 102-103, (2010/12/17)

The present invention relates to novel compounds of formulae (I) and (II) and therapeutically acceptable salts thereof, their pharmaceutical compositions processes for making them and their use in therapeutic methods for treatment and/or prevention of var

Practical enzymatic desymmetrization of 2-(ethoxycarbonyl)propane-1,3-diyl dihexanoate and model cyclization for the A-D ring system of lysergic acid

Miyata, Sachiho,Kumamoto, Takuya,Ishikawa, Tsutomu

, p. 1420 - 1438 (2008/02/08)

Porcine pancreas lipase-catalyzed hydrolysis of symmetrical 2-(ethoxycarbonyl)propane-1,3-diyl dihexanoate, under the modified conditions of the Seebach protocol, afforded a desymmetrized monohexanoate in 40-51% yield with 91-94% ee, even in a gram-scale reaction. The absolute configuration of a half-hydrolyzed (-)-product was determined to be (R) by conversion to a known 2-methylpropane-1,3-diol derivative. Samarium iodide-induced radical cyclization of 2-oxo-3-phenylethylamine with a C4 unit on the N-atom, derived from the racemic monohexanoate, afforded a 3-phenylpiperidine derivative as a model construction of the A-D ring system of lysergic acid.

α-Aminated methyllithium by DTBB-catalysed lithiation of a N- (chloromethyl) carbamate

Ortiz, Javier,Guijarro, Albert,Yus, Miguel

, p. 4831 - 4842 (2007/10/03)

The reaction of O-tert-butyl-N-(chloromethyl)-N-methyl carbamate (1) with lithium powder and a catalytic amount of 4,4'-di-tert-butylbiphenyl (DTBB, 2.5 mol %) in the presence of different electrophiles [Me3SiCl, (i)BuCHO, (t)BuCHO, PhCHO, 4-MeOC6H4CHO, (CH2)4CO, MeCO(n)Pr, Et2CO, MeCO(CH2)2CH=CH2, PhCOMe, PhCO(n)Bu, Ph2CO] in THF at -78°C leads, after hydrolysis with water, to the expected functionalised carbamates 2. Carbamates 2 derived from carbonyl compounds are deprotected with hydrogen chloride (for aromatic aldehyde or ketone derivatives) or with a mixture of phenol and trimethylsilyl chloride (for aliphatic aldehyde derivatives) giving substituted 1,2-diols 4.

α-Nitrogenated organolithium compounds from α-amidomethyl and α-aminomethyl sulfones

Alonso, Diego A.,Alonso, Emma,Najera, Carmen,Ramon, Diego J.,Yus, Miguel

, p. 4835 - 4856 (2007/10/03)

Successive reaction of α-amidomethyl sulfones 7a,b, derived from primary amides, with n-butyllithium and primary alkyl bromides (CH2 = CHCH2Br, CH2 = CMeCH2Br, CH2 = CBrCH2Br, CH ≡ CCH

α-Nitrogenated organolithium compounds from N-(tosylmethyl)amides

Alonso, Diego A.,Alonso, Emma,Nájera, Carmen,Yus, Miguel

, p. 491 - 492 (2007/10/03)

Deprotonation of α-amido sulfones 7 with BunLi at -90°C followed by reaction with electrophiles leads, depending on the substitution on the amidic nitrogen to enamides 10 (secondary amides 7a,b) or functionalised α-amido sulfones 12 (tertiary amides 7c,d). Naphthalene-catalysed lithiation of tertiary α-amido sulfones 7c,d in the presence of electrophiles (Barbier conditions) at -78°C affords functionalised amides 13.

O-tert-butyl-N-(chloromethyl)-N-methyl carbamate as a source of the MeNHCH2- synthon

Guijarro, Albert,Ortiz, Javier,Yus, Miguel

, p. 5597 - 5600 (2007/10/03)

The reaction of O-tert-butyl-N-(chloromethyl)-N-methyl carbamate (1) with lithium powder and a catalytic amount of DTBB (2.5 mol %) in the presence of different electrophiles [Me3SiCl, Bu(i)CHO, Bu(t)CHO, PhCHO, (CH2)4CO, Et2CO, PhCOMe, Ph2CO] in THF at -78°C leads, after hydrolysis with water, to the expected functionalised carbamates 2. As an example, the hydrolysis of compound 2e with hydrogen chloride affords easy deprotection of the amine functionality yielding the corresponding 1,2-aminoalcohol 3e.

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