4316-65-8 Usage
Uses
Used in Organic Synthesis:
3,5,5-TRIMETHYL-1-HEXENE is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of new compounds and materials.
Used in Chemical Production:
As a precursor, 3,5,5-TRIMETHYL-1-HEXENE is utilized in the production of a range of other chemicals, expanding its applications across different industries.
Used in Plastics Industry:
3,5,5-TRIMETHYL-1-HEXENE is used as a component in the manufacturing of plastics, contributing to the development of materials with specific properties for various applications.
Used in Coatings Industry:
3,5,5-TRIMETHYL-1-HEXENE is used in the production of coatings, where its chemical properties enhance the performance and characteristics of the final product.
Used in Adhesives Industry:
3,5,5-TRIMETHYL-1-HEXENE is employed in the manufacturing of adhesives, improving their bonding capabilities and durability.
Used in Fragrance Industry:
3,5,5-TRIMETHYL-1-HEXENE is used as a fragrance ingredient in perfumes and personal care products, adding to their scent profiles and enhancing consumer appeal.
Used in Safety Precautions:
While 3,5,5-TRIMETHYL-1-HEXENE offers numerous applications, it is crucial to handle this chemical with care due to its flammable nature and potential to cause skin or eye irritation, ensuring safety in its use across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 4316-65-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,1 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4316-65:
(6*4)+(5*3)+(4*1)+(3*6)+(2*6)+(1*5)=78
78 % 10 = 8
So 4316-65-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H18/c1-6-8(2)7-9(3,4)5/h6,8H,1,7H2,2-5H3
4316-65-8Relevant academic research and scientific papers
Copper catalyzed magnesium-Barbier reaction for γ-selective alkyl-allyl coupling
Erdik, Ender,Ko?o?lu, Melike
, p. 4211 - 4214 (2008/02/08)
CuCN catalyzed alkyl-allyl coupling under magnesium-Barbier conditions occurs regioselectively and affords predominantly the γ-products in good to high yields. This one-pot CuCN catalyzed reaction utilising Mg, an alkyl halide and an allylic substrate in THF at room temperature provides an easy alternative to the classical CuCN catalyzed γ-allylation of alkyl Grignard reagents.
