5908-40-7 Usage
Description
N~2~-(phenylacetyl)-N-(4-phenyl-1,3-thiazol-2-yl)-N~2~-propylglycinamide is a complex organic compound with a unique molecular structure. It is characterized by the presence of phenylacetyl, phenylthiazol, and propylglycinamide groups, which contribute to its chemical properties and potential applications.
Uses
Used in Pharmaceutical Industry:
N~2~-(phenylacetyl)-N-(4-phenyl-1,3-thiazol-2-yl)-N~2~-propylglycinamide is used as a pharmaceutical compound for its potential therapeutic effects. N~2~-(phenylacetyl)-N-(4-phenyl-1,3-thiazol-2-yl)-N~2~-propylglycinamide's structure allows it to interact with various biological targets, making it a candidate for the development of new drugs.
Used in Chemical Synthesis:
In the field of organic chemistry, N~2~-(phenylacetyl)-N-(4-phenyl-1,3-thiazol-2-yl)-N~2~-propylglycinamide can be used as a starting material or intermediate in the synthesis of other complex organic molecules. Its unique structure enables it to participate in various chemical reactions, such as substitution, elimination, and condensation reactions.
Used in Research and Development:
Due to its novel structure and potential applications, N~2~-(phenylacetyl)-N-(4-phenyl-1,3-thiazol-2-yl)-N~2~-propylglycinamide is also used in research and development for the exploration of new chemical reactions, drug discovery, and the development of new materials.
Physical properties:
The physical properties of N~2~-(phenylacetyl)-N-(4-phenyl-1,3-thiazol-2-yl)-N~2~-propylglycinamide may include characteristics such as solubility, melting point, and boiling point, which can be relevant for its handling, storage, and application in various industries.
Preparation
The best procedure for the preparation
of trimethylsilylacetone is the reaction of trimethylsilylmethylmagnesium
chloride or bromide with acetic anhydride.5
Other useful preparative methods for α-trimethylsilyl ketones
involve the reaction of trimethylsilylmethylmagnesium chloride
with acid chlorides,6 or with aldehydes followed by oxidation
of the resulting β-hydroxysilane to the ketone.2e When the
trialkylsilyl group is very large, particularly the triisopropylsilyl
group, a rearrangement from the silyl enol ether to the α-silyl
ketone is possible.
Check Digit Verification of cas no
The CAS Registry Mumber 5908-40-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,0 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5908-40:
(6*5)+(5*9)+(4*0)+(3*8)+(2*4)+(1*0)=107
107 % 10 = 7
So 5908-40-7 is a valid CAS Registry Number.
5908-40-7Relevant articles and documents
Acetylsilane O-Silylcyanohydrins as Precursors to α-Silyl Ketones and β-Siloxy-N,N-bissilylenamines
Cunico, Robert F.,Kuan, Chia P.
, p. 4634 - 4638 (2007/10/02)
Reduction of acetylsilane O-silylcyanohydrins gave β-amino-α-hydroxysilanes, which were diazotized to give α-silyl ketones.The addition of organolithium reagents to the cyanohydrins was accompanied by sequential C -> N and O -> N silyl group migrations.Silylation of the resulting lithium enolates afforded β-siloxy-N,N-bissilylenamines.
