104821-32-1 Usage
Description
2-(diMethoxyMethylsilyl)-bicyclo[2,2,1]heptanes are a class of organic chemicals characterized by a bicyclic structure with a silicon atom bonded to a dimethoxymethyl group. These compounds are known for their unique properties conferred by the silicon atom, which makes them valuable in organic chemistry. Their stable and relatively inert nature, along with their ability to selectively protect functional groups and facilitate specific chemical reactions, renders them useful in the synthesis of complex natural products and pharmaceuticals.
Uses
Used in Organic Synthesis:
2-(diMethoxyMethylsilyl)-bicyclo[2,2,1]heptanes serve as versatile reagents in organic synthesis, contributing to the formation of various complex organic molecules. Their presence aids in the selective protection of certain functional groups, which is crucial for multi-step synthesis processes.
Used as Protective Groups for Alcohols and Amines:
In the chemical industry, 2-(diMethoxyMethylsilyl)-bicyclo[2,2,1]heptanes are utilized as protective groups for alcohols and amines. This application is significant as it allows chemists to temporarily mask these functional groups during reactions, preventing unwanted side reactions and ensuring the desired product formation.
Used in the Synthesis of Complex Natural Products and Pharmaceuticals:
Due to their ability to selectively protect functional groups and facilitate specific chemical reactions, 2-(diMethoxyMethylsilyl)-bicyclo[2,2,1]heptanes are employed in the synthesis of complex natural products and pharmaceuticals. Their use in these applications helps in the development of new drugs and the exploration of novel chemical entities with potential therapeutic benefits.
Used as Precursors for Reactive Intermediates in Organic Transformations:
The stable and relatively inert nature of 2-(diMethoxyMethylsilyl)-bicyclo[2,2,1]heptanes makes them suitable precursors for generating reactive intermediates in organic transformations. This application is vital for advancing the field of organic chemistry by enabling the creation of new reaction pathways and the synthesis of previously inaccessible compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 104821-32-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,2 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104821-32:
(8*1)+(7*0)+(6*4)+(5*8)+(4*2)+(3*1)+(2*3)+(1*2)=91
91 % 10 = 1
So 104821-32-1 is a valid CAS Registry Number.
