114300-89-9 Usage
Molecular structure
A cyclohexadiene ring with two isopropyl groups (C3H7) attached to the 1 and 4 positions
Physical state
Colorless liquid
Odor
Sweet aromatic
Uses
a. Solvent in various industrial processes
b. Intermediate in the production of dyes, flavorings, and fragrances
Flammability
Flammable
Hazards
a. Skin irritation
b. Eye irritation
c. Respiratory system irritation
Safety precautions
Handle and store with caution to avoid potential hazards
Check Digit Verification of cas no
The CAS Registry Mumber 114300-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,0 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 114300-89:
(8*1)+(7*1)+(6*4)+(5*3)+(4*0)+(3*0)+(2*8)+(1*9)=79
79 % 10 = 9
So 114300-89-9 is a valid CAS Registry Number.
114300-89-9Relevant articles and documents
Asymmetric [3 + 2] cycloaddition of 2,3-butadienoates with electron-deficient olefins catalyzed by novel chiral 2,5-dialkyl-7-phenyl-7-phosphabicyclo[2.2.1]heptanes
Zhu,Chen,Jiang,Xiao,Cao,Zhang
, p. 3836 - 3837 (1997)
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Synthesis of optically active 2,5-dialkylcyclohexane-1,4-diols and their application in the asymmetric oxidation of sulfides
Sun, Jiangtao,Yang, Minghua,Dai, Zhenya,Zhu, Chengjian,Hu, Hongwen
scheme or table, p. 2513 - 2518 (2009/04/11)
A simple and efficient approach to obtain optically pure 1,4-diols was established. The asymmetric oxidation of sulfides to sulfoxides with cumyl hydroperoxide in moderate yields and moderate to high enantioselectivities (up to 84%) catalyzed by chiral Ti/ 1,4-diols complexes has been achieved. A 76% ee value was obtained in the asymmetric synthesis of esomeprazole. Georg Thieme Verlag Stuttgart.
