53750-52-0 Usage
Description
4-Iodo-2-methylbut-1-ene is an organic compound characterized by its unique structure, which features an iodine atom at the fourth carbon position, a methyl group at the second carbon position, and a double bond at the first carbon position. 4-iodo-2-methylbut-1-ene is known for its reactivity and is commonly utilized in various chemical reactions and synthesis processes.
Uses
Used in Chemical Synthesis:
4-Iodo-2-methylbut-1-ene is used as a reagent for the synthesis of functionalized cyclic boronates. Its unique structure and reactivity make it a valuable component in the creation of these compounds, which have a wide range of applications in various fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Iodo-2-methylbut-1-ene is used as a building block for the development of new drugs. Its ability to participate in various chemical reactions allows researchers to create novel molecular structures with potential therapeutic properties.
Used in Material Science:
4-Iodo-2-methylbut-1-ene is also utilized in the field of material science, where it can be used to synthesize new materials with specific properties. These materials may have applications in areas such as electronics, energy storage, and advanced coatings.
Used in Research and Development:
Due to its unique structure and reactivity, 4-Iodo-2-methylbut-1-ene is often used in research and development laboratories. It serves as a key component in the synthesis of various compounds, allowing scientists to explore new chemical reactions and develop innovative applications.
Check Digit Verification of cas no
The CAS Registry Mumber 53750-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,5 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53750-52:
(7*5)+(6*3)+(5*7)+(4*5)+(3*0)+(2*5)+(1*2)=120
120 % 10 = 0
So 53750-52-0 is a valid CAS Registry Number.
53750-52-0Relevant articles and documents
SECO-AMBRAKETALS
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, (2022/04/03)
The present invention primarily relates to compounds of formula (I) and compositions comprising one, two, three or more compound(s) of formula (I) or consisting of two, three or more compound(s) of formula (I). The invention further relates to methods for producing a compound of formula (I) or a composition as defined herein, the use of a compound of formula (I) as defined herein as a fragrance substance, the use of a composition as defined herein as a fragrance substance mixture and the use of a compound of formula (I) or a composition as defined herein for imparting, modifying and/or enhancing one or more olfactory notes selected from the group consisting of the notes ambergris, woody and animalic. Moreover, the present invention relates to fragrance substance compositions and perfumed products as defined herein, methods for producing a perfumed product, methods for perfuming a product and methods for perfuming hair, skin, textile fibres, surfaces and/or ambient air.
Synthetic studies toward jatrophane diterpenes from Euphorbia characias. enantioselective synthesis of (-)-15-O-Acetyl-3-O-propionyl-17-norcharaciol
Helmboldt, Hannes,Hiersemann, Martin
scheme or table, p. 1698 - 1708 (2009/10/02)
The enantioselective synthesis of (+)-17-norcharaciol is described. An uncatalyzed intramolecular carbonyl-ene reaction and a ring-closing metathesis were used as key C/C-connecting transformations to assemble the trans-bicyclo[10.3.0]pentadecane norditerpenoid core. We also report the evolution of our synthetic strategy toward the fully substituted characiol skeleton and the experiences from this venture.
Studies on the alkylation of 3-methyl-3-buten-1-ol dianion: An efficient synthesis of 3-methylene-1-alkanols including a San Jose scale sex pheromone
Yong, Kelvin H.,Lotoski, John A.,Chong, J. Michael
, p. 8248 - 8251 (2007/10/03)
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