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Tert-butyl (6-(hydroxyMethyl)pyriMidin-4-yl)carbaMate is a carbamate derivative with the molecular formula C11H18N4O3. It is a chemical compound that features a tert-butyl group, a pyrimidine ring, and a carbamate functional group. This versatile building block is commonly used in the pharmaceutical industry, particularly as a precursor in the synthesis of various pharmaceutical drugs. Its properties and reactivity make it a valuable tool for drug design and development, as well as for academic research in the field of medicinal chemistry.

954097-20-2

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954097-20-2 Usage

Uses

Used in Pharmaceutical Industry:
Tert-butyl (6-(hydroxyMethyl)pyriMidin-4-yl)carbaMate is used as a precursor in the synthesis of various pharmaceutical drugs for its ability to contribute to the creation of more complex chemical structures. Its presence in the molecular structure of drugs aids in enhancing their therapeutic effects and properties.
Used in Drug Design and Development:
Tert-butyl (6-(hydroxyMethyl)pyriMidin-4-yl)carbaMate is used as a building block in drug design and development due to its versatile nature and reactivity. It allows researchers and chemists to create new drug candidates with improved efficacy and safety profiles.
Used in Medicinal Chemistry Research:
Tert-butyl (6-(hydroxyMethyl)pyriMidin-4-yl)carbaMate is used as a valuable tool in academic research within the field of medicinal chemistry. Its unique structure and functional groups provide insights into the development of novel therapeutic agents and contribute to the advancement of pharmaceutical science.

Check Digit Verification of cas no

The CAS Registry Mumber 954097-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,4,0,9 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 954097-20:
(8*9)+(7*5)+(6*4)+(5*0)+(4*9)+(3*7)+(2*2)+(1*0)=192
192 % 10 = 2
So 954097-20-2 is a valid CAS Registry Number.

954097-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Carbamic acid, N-[6-(hydroxymethyl)-4-pyrimidinyl]-, 1,1-dimethylethyl ester

1.2 Other means of identification

Product number -
Other names TERT-BUTYL (6-(HYDROXYMETHYL)-PYRIMIDIN-4-YL)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:954097-20-2 SDS

954097-20-2Downstream Products

954097-20-2Relevant academic research and scientific papers

AZABENZOTHIAZOLE COMPOUNDS, COMPOSITIONS AND METHODS OF USE

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Page/Page column 85, (2012/04/04)

Provided are compounds of Formula I, stereoisomers, tautomers, solvates, prodrugs and pharmaceutically acceptable salts thereof, wherein A, X, R1, R2, R4 and R5 are defined herein, a pharmaceutical composition that includes a compound of Formula I and a pharmaceutically acceptable carrier, adjuvant or vehicle, methods of using the compound or composition in therapy, and methods of 5 manufacturing a compound of Formula I

Oxidation of methyl heteroaryls with molecular oxygen: A facile synthesis of 2-[N-(tert-butoxycarbonyl)amino]-4-pyridinecarbaldehyde

Berlin, Michael,Aslanian, Robert,Ruiz, Manuel De Lera,McCormick, Kevin D.

, p. 2529 - 2533 (2008/03/11)

Oxidation of nitrogen-based methyl heteroaryls with molecular oxygen resulted in the formation of the corresponding benzyl alcohols. While experimentally easy and amenable to large-scale preparations, this approach has limitations with respect to the particular nature of heterocyclic substrates. Using this methodology, the title compound, 2-[N-(tert-butoxycarbonyl)amino]-4- pyridinecarbaldehyde, considered to be a versatile pharmaceutical intermediate, was prepared on a multigram scale. Georg Thieme Verlag Stuttgart.

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