526221-24-9 Usage
Description
(S)-2-Azido-2-methyl-3-phenyl-propionaldehyde is a chemical compound characterized by its molecular formula C10H11N3O. It is a chiral aldehyde featuring an azido group, a methyl group, and a phenyl group attached to a propionaldehyde moiety. (S)-2-Azido-2-methyl-3-phenyl-propionaldehyde is known for its versatility in organic synthesis and is a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. The azido functional group in (S)-2-Azido-2-methyl-3-phenyl-propionaldehyde makes it a valuable building block for the synthesis of diverse nitrogen-containing compounds. Furthermore, its chiral nature is advantageous for asymmetric synthesis and the creation of enantiopure compounds. However, due to its potential reactivity and explosive nature, (S)-2-Azido-2-methyl-3-phenyl-propionaldehyde should be handled with caution.
Uses
Used in Pharmaceutical Industry:
(S)-2-Azido-2-methyl-3-phenyl-propionaldehyde is used as a key intermediate for the synthesis of various pharmaceuticals. Its azido functional group and chiral nature make it a valuable building block for creating nitrogen-containing compounds and enantiopure drugs, which are essential in the development of new medications.
Used in Agrochemical Industry:
In the agrochemical industry, (S)-2-Azido-2-methyl-3-phenyl-propionaldehyde is utilized as an intermediate for the production of various agrochemicals. Its unique structure and functional groups contribute to the development of new compounds with potential applications in agriculture, such as pesticides and herbicides.
Used in Specialty Chemicals Industry:
(S)-2-Azido-2-methyl-3-phenyl-propionaldehyde is also used in the specialty chemicals industry for the synthesis of a wide range of nitrogen-containing compounds. Its versatility as a building block allows for the creation of various specialty chemicals with specific applications in different fields, such as materials science, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 526221-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,6,2,2 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 526221-24:
(8*5)+(7*2)+(6*6)+(5*2)+(4*2)+(3*1)+(2*2)+(1*4)=119
119 % 10 = 9
So 526221-24-9 is a valid CAS Registry Number.
526221-24-9Relevant articles and documents
Stereospecific construction of chiral quaternary carbon compounds from chiral secondary alcohol derivatives
Masaki, Yukio,Arasaki, Hideki,Iwata, Masashi
, p. 4 - 5 (2007/10/03)
Chiral tertiary dichloromethylcarbinol derivatives, prepared by stereospecific α C-H insertion reaction of dichlorocarbene with protected chiral secondary alcohols, were converted into intermediary α-chloroepoxides which gave stereospecifically chiral qua
