31206-61-8 Usage
Physical Properties
Color: Colorless
Odor: Odorless
Toxicity: Non-toxic
State: Liquid
Solubility: Insoluble in water
Main Uses
Building block in polyester resins, polyurethanes, and other polymers
Enhances durability, flexibility, and chemical resistance of materials
Manufacturing coatings, adhesives, and lubricants
Advantages
Low volatility
Stability
Industrial Importance
Versatile and important industrial chemical
Check Digit Verification of cas no
The CAS Registry Mumber 31206-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,0 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 31206-61:
(7*3)+(6*1)+(5*2)+(4*0)+(3*6)+(2*6)+(1*1)=68
68 % 10 = 8
So 31206-61-8 is a valid CAS Registry Number.
31206-61-8Relevant academic research and scientific papers
Synthesis of (±)-trans-2,5-diisopropylborolane
Laschober, Gerhard,Zorzi, Massimo,Hodgetts, Kevin J.
, p. 244 - 252 (2007/10/03)
The cyclic hydroboration of 2,7-dimethyl-2,6-octadiene (6) was studied. It was found that the stereochemical outcome of the reaction was dependent upon the solvent, temperature, time and the nature of the borane reagent. Pure racemic trans-2,5-diisopropyl
Remote Stereocontrol by utilizing Intramolecular Carbonyl Reduction with Boranes
Harada, Toshiro,Matsuda, Yasuhiro,Imanaka, Satoru,Oku, Akira
, p. 1641 - 1643 (2007/10/02)
A simple and efficient method for the remote (1,4- and/or 1,5-) stereocontrol was realized by utilizing an intramolecular carbonyl reduction with ThexBH2 (Thex = 1,1,2-trimethylpropyl).
