906453-98-3 Usage
Description
(R)-3-(Benzyloxy)hex-5-enamide, with the chemical formula C16H19NO2, is a chiral compound characterized by its non-superimposable mirror image. The (R) designation signifies the absolute configuration of the molecule. (R)-3-(BENZYLOXY)HEX-5-ENAMIDE features a hex-5-enamide group, which consists of a primary amide attached to a 5-carbon chain with a double bond, and a benzyloxy group, where a benzene ring is connected to an oxygen atom that is, in turn, attached to the 3-carbon of the chain. Its unique structure and potential biological activity make it a compound of interest for applications in organic synthesis and pharmaceutical research.
Uses
Used in Organic Synthesis:
(R)-3-(Benzyloxy)hex-5-enamide is used as an intermediate in the synthesis of various organic compounds due to its unique structural features. The presence of the amide and benzyloxy groups allows for further functionalization and modification, making it a versatile building block in the creation of complex organic molecules.
Used in Pharmaceutical Research:
(R)-3-(Benzyloxy)hex-5-enamide is used as a starting material or a key intermediate in the development of new pharmaceuticals. Its potential biological activity and unique structure make it a promising candidate for the design and synthesis of novel drugs targeting specific therapeutic areas.
Used in Chemical Research:
(R)-3-(Benzyloxy)hex-5-enamide serves as a valuable compound for studying the reactivity and properties of amide and benzyloxy groups. It can be used to investigate various chemical reactions, such as substitution, addition, and elimination, providing insights into the behavior of similar compounds and contributing to the broader understanding of organic chemistry.
Used in Analytical Chemistry:
(R)-3-(Benzyloxy)hex-5-enamide can be employed as a chiral reference standard in analytical chemistry. Its distinct (R) configuration allows for the accurate determination of enantiomeric purity and the study of stereoselective reactions, which are crucial in the development of enantiomerically pure compounds with specific biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 906453-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,4,5 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 906453-98:
(8*9)+(7*0)+(6*6)+(5*4)+(4*5)+(3*3)+(2*9)+(1*8)=183
183 % 10 = 3
So 906453-98-3 is a valid CAS Registry Number.
906453-98-3Relevant articles and documents
Eight-step synthesis of routiennocin
Matsumotoa, Kenji,Kozmina, Sergey A.
supporting information; experimental part, p. 557 - 560 (2009/04/11)
Routiennocin is a member of a family of polycyclic pyrrole ether antibiotics that simultaneously uncouple oxidative phosphorylation and inhibit ATPase as a result of selective complexation of divalent metal ions. We describe a concise synthesis of routien
Dramatic enhancement of enantioselectivity of biotransformations of β-hydroxy nitriles using a simple O-benzyl protection/docking group
Ma, Da-You,Zheng, Qi-Yu,Wang, De-Xian,Wang, Mei-Xiang
, p. 3231 - 3234 (2007/10/03)
Catalyzed by the Rhodococcus erythropolis AJ270 whole cell catalyst, the O-benzylated β-hydroxy alkanenitriles underwent remarkably high enantioselective biotransformations, whereas the biotransformations of free β-hydroxy alkanenitriles gave very low ena
