2975-46-4 Usage
Description
3-Trimethylsilylpropynal is an organic compound characterized by its unique structure and properties. It is known for its versatility as an intermediate in various chemical reactions and synthesis processes.
Uses
Used in Agrochemicals:
3-Trimethylsilylpropynal is used as an intermediate in the agrochemical industry for the synthesis of various pesticides and other agricultural chemicals. Its unique reactivity allows for the creation of compounds with specific properties that can be tailored to target pests and improve crop yields.
Used in Pharmaceuticals:
In the pharmaceutical industry, 3-Trimethylsilylpropynal serves as a key intermediate in the synthesis of various drugs and medicinal compounds. Its ability to participate in a range of chemical reactions makes it a valuable component in the development of new pharmaceuticals with improved efficacy and reduced side effects.
Used in Dyestuff:
3-Trimethylsilylpropynal is also utilized in the dyestuff industry, where it is employed as an intermediate for the production of various dyes and pigments. Its unique chemical properties enable the creation of dyes with specific color characteristics and improved stability.
Used in the Preparation of [3-(trimethylsilyl)-2-propinyliden]-malononitrile:
3-Trimethylsilylpropynal is used in the preparation of [3-(trimethylsilyl)-2-propinyliden]-malononitrile, a compound with potential applications in various industries, including the synthesis of advanced materials and specialty chemicals. Its role in this process highlights its importance as a versatile intermediate in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 2975-46-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2975-46:
(6*2)+(5*9)+(4*7)+(3*5)+(2*4)+(1*6)=114
114 % 10 = 4
So 2975-46-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H10OSi/c1-8(2,3)6-4-5-7/h5H,1-3H3
2975-46-4Relevant articles and documents
Reactivity of indole-3-alkoxides in the absence of acids: Rapid synthesis of homo-bisindolylmethanes
Chinta, Bhavani Shankar,Baire, Beeraiah
, p. 8106 - 8116 (2016/11/22)
An unprecedented behaviour of in situ generated indole-3-alkoxides (MgX or Li) has been reported. Tuning the electronic properties of the alkoxides offered the direct and selective construction of bisindolylmethanes and indole-3-carbinols. This process shows very broad scope and represents the reagent (external) free, greener synthesis of structurally divergent bisindolylmethanes.
