85895-82-5 Usage
Uses
Used in Synthetic Rubber Production:
(1,2,3-trimethylbut-3-enyl)benzene is used as a monomer in the production of polyisoprene, a synthetic rubber that exhibits properties akin to natural rubber. This makes it a valuable component in the creation of synthetic rubbers with a wide range of applications.
Used in Elastomer Production:
Isodurene serves as a key ingredient in the manufacturing of elastomers, which are essential for producing flexible and durable materials used in various industries.
Used in Adhesives:
(1,2,3-trimethylbut-3-enyl)benzene is utilized in the production of adhesives, contributing to the development of strong and reliable bonding agents for different types of materials.
Used in Coatings:
Isodurene is also employed in the formulation of coatings, enhancing the performance and durability of surface treatments in various applications.
Safety Precautions:
Given its flammable and volatile nature, it is crucial to handle (1,2,3-trimethylbut-3-enyl)benzene with care and adhere to proper safety measures during its use and storage.
Check Digit Verification of cas no
The CAS Registry Mumber 85895-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,9 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 85895-82:
(7*8)+(6*5)+(5*8)+(4*9)+(3*5)+(2*8)+(1*2)=195
195 % 10 = 5
So 85895-82-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H18/c1-10(2)11(3)12(4)13-8-6-5-7-9-13/h5-9,11-12H,1H2,2-4H3
85895-82-5Relevant academic research and scientific papers
The Diastereoselectivity of Electrophilic Attack on Trigonal Carbon Adjacent to a Stereogenic Centre: Diastereoselective Protonation, Epoxidation and Acylation of Allylsilanes
Fleming, Ian,Lewis, Jeremy J.
, p. 3267 - 3276 (2007/10/02)
The four allylsilanes 6 and 8, which have a stereogenic centre carrying a phenyl group, a methyl group and a hydrogen atom adjacent to the nucleophilic end of the double bond, react with protic (or deuteronic) acid, m-chloroperbenzoic acid and chlorosulfonyl isocyanate to give eletrophilic substitution of the allylsilane, with diastereoselectivity in the sense 2, in conformity to a general rule for electrophilic attack on a double bond adjacent to a stereogenic centre.The most reliably stereoselective reactions took place with the allylsilane 6b, in which the stereogenic centre is cis to a group larger than a hydrogen atom in both the E- and Z-isomer.In general, chlorosulfonyl isocyanate induces higher stereoselectivity than the peracid, and the peracid higher stereoselectivity than the proton (or deuteron).
