681-98-1 Usage
Description
Titanium(IV) isobutoxide, with the chemical formula Ti[OCH(CH3)2]4, is a colorless-to-pale-yellow liquid characterized by a strong odor. It is a highly reactive and flammable precursor in the synthesis of titanium-based materials, such as titanium dioxide and titanium alkoxides. Due to its reactivity, it requires careful handling.
Used in Chemical Synthesis:
Titanium(IV) isobutoxide is used as a precursor in the synthesis of titanium-based materials for various applications, including the production of titanium dioxide and titanium alkoxides.
Used in Organic Synthesis:
It is utilized as a catalyst in organic synthesis processes, facilitating specific chemical reactions and improving the efficiency of the synthesis.
Used in Polymer Production:
Titanium(IV) isobutoxide is employed as a cross-linking agent in the production of polymers, enhancing their structural integrity and performance.
Used in Coatings and Adhesives Industry:
It is used as a component in the production of coatings and adhesives, where its unique properties as a titanium compound contribute to the quality and performance of these materials.
Used in Material Production:
Titanium(IV) isobutoxide is an important industrial chemical with applications in the production of various materials, capitalizing on its distinctive characteristics as a titanium compound.
Check Digit Verification of cas no
The CAS Registry Mumber 681-98-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 681-98:
(5*6)+(4*8)+(3*1)+(2*9)+(1*8)=91
91 % 10 = 1
So 681-98-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H36O4Si/c1-13(2)9-17-21(18-10-14(3)4,19-11-15(5)6)20-12-16(7)8/h13-16H,9-12H2,1-8H3
681-98-1Relevant articles and documents
Reaction of silicon with alcohols in autoclave
Krylova,Egorov,Nefedov
, p. 260 - 266 (2017/07/11)
A reaction of activated silicon with alcohols in an autoclave at 240—270 °C was studied. It was found that primary alcohols form tetraalkoxysilanes Si(OR)4 with high selectivity (up to 97%), while the secondary PriOH gave a mixture of compounds HSi(OPri)3, Si(OPri)4, HSi(OPri)2OSi(OPri)2H, HSi(OPri)2OSi(OPri)3, and Si(OPri)3OSi(OPri)3 with the predominance of trialkoxysilane (up to 67%). Carrying out the reaction under the indicated conditions has the advantage of experimental simplicity, reagent availability, high conversion of silicon, good isolated yields of products.