105532-86-3 Usage
Uses
Used in Pharmaceutical Synthesis:
N-METHOXY-N,O-BIS(TRIMETHYLSILYL)CARBAMATE is used as a protecting agent for amines in the synthesis of various pharmaceuticals. Its ability to shield reactive amines allows for the successful synthesis of complex drug molecules without unwanted side reactions.
Used in Fine Chemicals Synthesis:
In the production of fine chemicals, N-METHOXY-N,O-BIS(TRIMETHYLSILYL)CARBAMATE is used as a protective group for amines to ensure the purity and yield of the final product. Its steric hindrance and stability are essential for the synthesis of high-quality fine chemicals.
Used in Material Development:
N-METHOXY-N,O-BIS(TRIMETHYLSILYL)CARBAMATE is utilized as a protective agent in the development of new materials, where the protection of amines is crucial for the successful synthesis of innovative material compounds.
Used in Organic Chemistry Research:
In the field of organic chemistry research, N-METHOXY-N,O-BIS(TRIMETHYLSILYL)CARBAMATE is used as a tool for amine protection, facilitating the exploration of new reaction pathways and the synthesis of novel organic compounds. Its mild removal conditions allow for the controlled deprotection of amines, which is vital for the advancement of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 105532-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,3 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 105532-86:
(8*1)+(7*0)+(6*5)+(5*5)+(4*3)+(3*2)+(2*8)+(1*6)=103
103 % 10 = 3
So 105532-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H21NO3Si2/c1-11-9(13(2,3)4)8(10)12-14(5,6)7/h1-7H3
105532-86-3Relevant academic research and scientific papers
Trimethylsilylcarbamates and a process for the preparation thereof
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, (2008/06/13)
The invention relates to new compounds of the general formulae (I) and/or (II), STR1 wherein R1 is a C1-6 alkyl or an aralkyl group, and R2 is hydrogen or a C1-6 alkyl group. According to another aspect of the invention there are provided processes for the preparation of these compounds. The compounds of the general formulae (I) and/or (II) are utilizable for the oxymation and/or trimethylsilylation of any substrate bearing an oxo group and/or a silylable polar hydrogen. The compounds of the general formula (VI): wherein R1 is as defined above Y is oxygen, nitrogen or sulphur atom or a carboxylate anion, and Z is the skeleton of the substrate, said compounds being formed in the oxymation and/or trimethylsilylation reaction, are also within the scope of the invention.
