218608-93-6 Usage
Description
BOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID is a chiral chemical compound with the molecular formula C14H18ClNO4. It is a derivative of 3-amino-4-(2-chloro-phenyl)butyric acid, featuring a Boc (tert-butyloxycarbonyl) protecting group. BOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID is widely used in organic synthesis and pharmaceutical research, serving as a valuable building block for the synthesis of pharmaceutical drugs and other biologically active compounds. Its importance lies in drug discovery and development, as well as in academic and industrial research within the realm of organic chemistry.
Uses
Used in Pharmaceutical Research:
BOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID is used as a key intermediate in the synthesis of pharmaceutical drugs due to its unique chemical structure and chiral properties. The Boc protecting group allows for selective reactions and the preparation of various chiral compounds, which are essential in the development of enantiomerically pure drugs with desired therapeutic effects and minimized side effects.
Used in Organic Synthesis:
In the field of organic synthesis, BOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID serves as a versatile building block for the creation of complex organic molecules. Its reactivity and functional groups enable the formation of a wide range of chemical products, including biologically active compounds, which can be further utilized in various applications such as agrochemicals, fragrances, and dyes.
Used in Drug Discovery:
BOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID is employed as a starting material in drug discovery processes. Its unique structure and properties make it a promising candidate for the development of new pharmaceutical agents with novel mechanisms of action. Researchers can modify and optimize its structure to explore its potential as a therapeutic agent for various diseases and conditions.
Used in Academic Research:
In academic research, BOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID is utilized to study various aspects of organic chemistry, including reaction mechanisms, stereochemistry, and the synthesis of complex organic molecules. Its unique properties and reactivity provide valuable insights into the fundamental principles of organic chemistry and contribute to the advancement of the field.
Used in Industrial Research:
BOC-(R)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID is also used in industrial research for the development of new processes and technologies in the chemical and pharmaceutical industries. Its applications extend beyond drug synthesis, as it can be employed in the production of specialty chemicals, materials, and other products that require chiral compounds with specific properties.
Check Digit Verification of cas no
The CAS Registry Mumber 218608-93-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,6,0 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 218608-93:
(8*2)+(7*1)+(6*8)+(5*6)+(4*0)+(3*8)+(2*9)+(1*3)=146
146 % 10 = 6
So 218608-93-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H20ClNO4/c1-15(2,3)21-14(20)17-11(9-13(18)19)8-10-6-4-5-7-12(10)16/h4-7,11H,8-9H2,1-3H3,(H,17,20)(H,18,19)/t11-/m1/s1
