83704-03-4 Usage
Uses
Used in Coatings Industry:
3-[(1,1-dimethylethoxy)methyl]heptane is used as a solvent for the production of coatings, aiding in the application process and enhancing the final product's quality.
Used in Adhesives Industry:
In the adhesives industry, 3-[(1,1-dimethylethoxy)methyl]heptane is used as a solvent to improve the adhesive's performance and facilitate its application.
Used in Cleaning Products Industry:
3-[(1,1-dimethylethoxy)methyl]heptane is used as a solvent in cleaning products, contributing to their effectiveness in removing dirt and stains.
Used as a Versatile Solvent:
Due to its ability to dissolve a wide range of substances, 3-[(1,1-dimethylethoxy)methyl]heptane is used as a versatile and effective solvent in various industrial processes, making it a valuable ingredient in the manufacturing of different products across multiple industries.
Check Digit Verification of cas no
The CAS Registry Mumber 83704-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,0 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83704-03:
(7*8)+(6*3)+(5*7)+(4*0)+(3*4)+(2*0)+(1*3)=124
124 % 10 = 4
So 83704-03-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H26O/c1-6-8-9-11(7-2)10-13-12(3,4)5/h11H,6-10H2,1-5H3
83704-03-4Relevant academic research and scientific papers
Gold(I)-catalyzed synthesis of unsymmetrical ethers using alcohols as alkylating reagents
Liu, Yongxiang,Wang, Xiaoyu,Wang, Yanshi,Du, Chuan,Shi, Hui,Jin, Shengfei,Jiang, Chongguo,Xiao, Jianyong,Cheng, Maosheng
, p. 1029 - 1036 (2015/03/30)
A microwave-irradiated alcohol-protecting strategy based on gold catalysis utilizing benzyl alcohol, tert-butyl alcohol and triphenylmethanol as alkylating reagents has been developed. This protecting strategy has wide functional group tolerance with satisfactory yields for the majority of the selected alcohols. The mechanism of this transformation was probed with oxygen-18 isotope labelled alcohols assisted by GC-MS techniques and chemical kinetic experiments. This strategy provides an efficient, straightforward and alternative approach to the preparation of benzyl, tert-butyl and trityl ethers in organic synthesis.
