6102-13-2 Usage
Type
Diethyl ester derivative of 1,3-cyclohexanedicarboxylic acid
Functional groups
Hydroxy group, two methyl groups, and a carbonyl group
Molecular Structure
Cyclohexane ring with two ester groups, hydroxy group, and two methyl groups
Pharmaceutical industry
Building block for the synthesis of various drugs and pharmaceuticals
Organic chemistry
Preparation of various functionalized cyclohexanes
Research and drug development
Potential biological activity
Industry
Chemical and pharmaceutical
Physical State
Likely a liquid or solid, depending on temperature and conditions
Solubility
Soluble in organic solvents, such as ethanol, methanol, or acetone
Stability
Stable under normal conditions, but sensitive to heat, light, or strong acids and bases
Reactivity
May react with nucleophiles, electrophiles, or other reagents to form various functionalized cyclohexanes
Safety
Handle with care, as it may have potential hazards or toxic effects
Storage
Store in a cool, dry, and well-ventilated area, away from heat, light, and strong acids or bases
Disposal
Dispose of according to local regulations and guidelines for chemical waste
Purity
Typically synthesized with high purity for use in pharmaceutical and chemical applications
Check Digit Verification of cas no
The CAS Registry Mumber 6102-13-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,0 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6102-13:
(6*6)+(5*1)+(4*0)+(3*2)+(2*1)+(1*3)=52
52 % 10 = 2
So 6102-13-2 is a valid CAS Registry Number.
6102-13-2Relevant academic research and scientific papers
Synthesis of highly functionalized 3,4-cyclohexane-annelated coumarins
Chen, Chao-Yue,Zhang, Xiao-Mei,Shi, Jian-Jun,He, Jie
, p. 583 - 593 (2015/03/04)
Efficient synthetic access to highly functionalized 3,4-cyclohexane-annelated coumarins has been achieved by combining two methods. First, the important intermediates multisubstituted cyclic ?2-keto esters were prepared conveniently by condensing a variet
13C and 1H NMR SPECTRA AND STRUCTURE OF THE PRODUCTS FROM THE CONDENSATION OF 1,3-DICARBONYL COMPOUNDS WITH ALDEHYDES
Emelina, E. E.,Gindin, V. A.,Ershov, B. A.
, p. 2263 - 2268 (2007/10/02)
The structure of the diadducts formed in the reaction of 1,3-dicarbonyl compounds with aldehydes in a ratio of 2:1 under the conditions of the Knoevenagel condensation was studied by 13C and 1H NMR spectroscopy.It was shown that acyclic tetracarbonyl comp
