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Carbamic acid, (2-hydroxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI) is a chemical compound that belongs to the ester class, which are organic compounds formed by the reaction of an acid with an alcohol. This specific compound is synthesized from carbamic acid and 2-hydroxy-2-methylpropyl, featuring a carbamic acid group (NH2COOH), a 2-hydroxy-2-methylpropyl group, and a 1,1-dimethylethyl ester group. Its molecular formula is C9H19NO3. Carbamic acid, (2-hydroxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI)'s potential applications in chemical research and various industries are determined by its unique chemical structure, although specific uses, hazards, or safety measures may require further testing and investigation.

183059-24-7

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183059-24-7 Usage

Uses

Used in Chemical Research:
Carbamic acid, (2-hydroxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI) is used as a research compound for studying its chemical properties and potential interactions with other substances. Its unique structure may offer insights into new chemical reactions or mechanisms.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Carbamic acid, (2-hydroxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI) may be used as an intermediate in the synthesis of various drugs or as a component in drug formulations. Its chemical properties could contribute to the development of new therapeutic agents.
Used in Agrochemical Industry:
Carbamic acid, (2-hydroxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI) could be utilized in the agrochemical industry as a component in the development of new pesticides or herbicides. Its chemical structure may provide a basis for creating more effective and environmentally friendly products.
Used in Material Science:
In material science, Carbamic acid, (2-hydroxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI) may be explored for its potential use in the creation of new materials or polymers. Its unique structure could contribute to the development of innovative materials with specific properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 183059-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,0,5 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 183059-24:
(8*1)+(7*8)+(6*3)+(5*0)+(4*5)+(3*9)+(2*2)+(1*4)=137
137 % 10 = 7
So 183059-24-7 is a valid CAS Registry Number.

183059-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(2-hydroxy-2-methylpropyl)carbamate

1.2 Other means of identification

Product number -
Other names tert-Butyl 2-hydroxy-2-methylpropylcarbamate

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:183059-24-7 SDS

183059-24-7Relevant academic research and scientific papers

INHIBITORS OF BETA-SECRETASE

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Paragraph 0161-0162, (2014/03/24)

The present invention relates to spirocyclic acylguanidines and their use as inhibitors of the β-secretase enzyme (BACE1) activity, pharmaceutical compositions containing the same, and methods of using the same as therapeutic agents in the treatment of neurodegenerative disorders, disorders characterized by cognitive decline, cognitive impairment, dementia and diseases characterized by production of β-amyloid aggregates.

INHIBITORS OF BETA-SECRETASE

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Page/Page column 29, (2013/09/26)

The present invention relates to spirocyclic acylguanidines and their use as inhibitors of the β-secretase enzyme (BACEl) activity, pharmaceutical compositions containing the same, and methods of using the same as therapeutic agents in the treatment of neurodegenerative disorders, disorders characterized by cognitive decline, cognitive impairment, dementia and diseases characterized by production of β-amyloid aggregates.

N-Phosphoryl oxazolidinones as effective phosphorylating agents

Jones, Simon,Smanmoo, Chaiwat

, p. 1585 - 1588 (2007/10/03)

A number of N-phosphoryl oxazolidinones have been prepared and evaluated, the best being 5,5-diphenyl oxazolidinones, the utility of which was demonstrated in the phosphorylation of a number of representative primary, secondary, tertiary, and phenolic alcohols.

N-acyl-5,5-dimethyl-oxazolidin-2-ones as latent aldehyde equivalents

Bach, Jordi,Bull, Steven D.,Davies, Stephen G.,Nicholson, Rebecca L.,Sanganee, Hitesh J.,Smith, Andrew D.

, p. 6677 - 6680 (2007/10/03)

N-acyl-5,5-dimethyl-oxazolidin-2-ones can function as versatile latent aldehyde equivalents - reductive cleavage with DIBAL-H affords aldehydes in good yield, while tandem DIBAL-H/Wittig methodology affords α,β-unsaturated esters.

Asymmetric alkylations using SuperQuat auxiliaries - An investigation into the synthesis and stability of enolates derived from 5,5-disubstituted oxazolidin-2-ones

Bull, Steven D.,Davies, Stephen G.,Jones, Simon,Sanganee, Hitesh J.

, p. 387 - 398 (2007/10/03)

Studies on the alkylation of enolates derived from a range of N-acyl-5,5-dimethyloxazolidin-2-ones and N-acyl-5,5-diphenyloxazolidin-2-ones reveal that high yields and high diastereoselectivities are best obtained when homochiral 4-isopropyl-5,5-dimethyloxazolidin-2-one is employed as a chiral auxiliary.

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