6429-44-3 Usage
Description
(S)-Benzyl (1-hydroxypropan-2-yl)carbamate, a carbamate derivative with a molecular formula C12H17NO3, features a benzyl group and a hydroxypropan-2-yl group attached to the carbamate function. As a chiral molecule, it has a stereocenter at the carbon atom bearing the carbamate group, leading to two enantiomers: the (S)and (R)forms. (S)-benzyl (1-hydroxypropan-2-yl)carbamate is known for its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and it also holds potential in organic chemistry for creating various organic compounds.
Uses
Used in Pharmaceutical Synthesis:
(S)-Benzyl (1-hydroxypropan-2-yl)carbamate is used as an intermediate for the synthesis of pharmaceutical compounds. Its unique structure allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, (S)-benzyl (1-hydroxypropan-2-yl)carbamate is utilized as an intermediate in the production of various agrochemicals, contributing to the development of effective solutions for agricultural needs.
Used in Organic Chemistry:
(S)-Benzyl (1-hydroxypropan-2-yl)carbamate serves as a building block in organic chemistry for the preparation of a wide range of organic compounds. Its versatile structure enables the creation of novel molecules with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 6429-44-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,2 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6429-44:
(6*6)+(5*4)+(4*2)+(3*9)+(2*4)+(1*4)=103
103 % 10 = 3
So 6429-44-3 is a valid CAS Registry Number.
6429-44-3Relevant articles and documents
Novel sulfonamide-based carbamates as selective inhibitors of bche
?těpánková, ?árka,Enriz, Ricardo D.,Garro, Adriana D.,Ho?ek, Jan,Imramovsky, Ale?,Jampílek, Josef,Jendrzejewska, Izabela,Magar, Pratibha,Parravicini, Oscar,Pauk, Karel,Svr?ková, Katarina
, (2021/09/04)
A series of 14 target benzyl [2-(arylsulfamoyl)-1-substituted-ethyl]carbamates was prepared by multi-step synthesis and characterized. All the final compounds were tested for their abil-ity to inhibit acetylcholinesterase (AChE) and butyrylcholinesterase
RHO KINASE INHIBITOR, METHOD FOR PREPARING SAME AND USES THEREOF
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Paragraph 0115, (2021/09/16)
Provided are a Rho kinase inhibitor, a method for preparing same and the uses thereof. The Rho kinase inhibitor designates a compound of Formula I, a stereoisomer thereof or pharmaceutically acceptable salt thereof. The Rho kinase inhibitor promotes endothelial cells and endothelin expression, prostenin expression, and vascular factors NO synthesis and secretion, has a promoting effect on proprostin expression independently of the doses used, shows lower toxicity, while being safer.
Chiral pyrazole derivative and synthesis method thereof
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Paragraph 0027-0029; 0040-0042; 0053-0055, (2020/06/20)
The invention belongs to the technical field of organic synthesis, and discloses a chiral pyrazole derivative and a synthesis method thereof. The chiral pyrazole derivative is (1-(4'-amino-5'-carbamoyl-1'-pyrazolyl)-(S)-2-propyl-benzyloxy amide. The synth
