93962-67-5 Usage
Category
Synthetic organic compound
It is artificially synthesized and belongs to the class of organic compounds.
Chirality
Chiral compound with two chiral centers
The compound has two centers of asymmetry, which means it can exist in different stereoisomers.
Derivative
Phenylpropanol
It is derived from the parent compound phenylpropanol, which is a type of alcohol.
Structural groups
p-chlorophenyl and 5-chloro-2-hydroxyphenyl
The compound contains two distinct functional groups, which are responsible for its chemical properties.
Potential applications
Pharmaceutical industry
It may be used as an intermediate in the synthesis of other chemical compounds, particularly in the pharmaceutical sector.
Research and development
Ongoing
Further research is needed to fully understand its specific properties and potential uses.
Solubility
Unknown (requires experimental data)
The solubility of the compound in various solvents is not provided and would need to be determined through experimentation.
Stability
Unknown (requires experimental data)
The stability of the compound under different conditions is not provided and would need to be determined through experimentation.
Reactivity
Unknown (requires experimental data)
The reactivity of the compound with other substances is not provided and would need to be determined through experimentation.
Check Digit Verification of cas no
The CAS Registry Mumber 93962-67-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,6 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93962-67:
(7*9)+(6*3)+(5*9)+(4*6)+(3*2)+(2*6)+(1*7)=175
175 % 10 = 5
So 93962-67-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H14Cl2O2/c16-12-4-1-10(2-5-12)14(18)7-3-11-9-13(17)6-8-15(11)19/h1-2,4-6,8-9,14,18-19H,3,7H2
93962-67-5Relevant articles and documents
A Modular Synthesis of 2-Alkyl- and 2-Arylchromans via a Three-Step Sequence
Orr, Robert K.,Campeau, Louis-Charles,Chobanian, Harry R.,McCabe Dunn, Jamie M.,Pio, Barbara,Plummer, Christopher W.,Nolting, Andrew,Ruck, Rebecca T.
, p. 657 - 666 (2017)
A convergent three-step method for the synthesis of 2-substituted chromans is described. These results have been accomplished via the Heck coupling of readily accessible allylic alcohols and 2-iodophenols, followed by reduction and Mitsunobu cyclization. The utility and generality of this method is demonstrated through the synthesis of a series of 2-aryl-, 2-heteroaryl- and 2-alkylchromans, as well as an azachroman derivative. The asymmetric version of this approach via a Noyori-catalyzed ketone reduction and subsequent cyclization is likewise highlighted.
