196871-46-2 Usage
Chemical Family
Aromatic compounds
Explanation
Different sources of media describe the Explanation of 196871-46-2 differently. You can refer to the following data:
1. Belongs to a group of compounds containing a benzene ring with delocalized electrons.
2. The compound is derived from benzene, a basic building block in organic chemistry.
3. The benzene ring has two hydroxyl (OH) groups attached to it.
4. The presence of ethyl groups (C2H5) attached to the carbon atoms next to the hydroxyl groups.
5. Used as a solvent, intermediate in chemical synthesis, and in the production of plastics, resins, pharmaceuticals, and medications.
6. The compound's chemical and physical properties make it valuable in various industrial applications.
7. The molecular formula represents the compound's composition of 10 carbon, 14 hydrogen, and 2 oxygen atoms.
8. As a solvent, it can dissolve a wide range of substances, making it useful in chemical reactions and processes.
9. The compound can undergo various chemical reactions, making it a useful intermediate in the synthesis of other chemicals.
10. The compound's physical state can vary depending on the temperature, which can affect its applications and handling.
Derived from
Benzene
Hydroxyl groups
Two
Alpha, alpha-diethyl substitution
Ethyl groups on adjacent carbon atoms
Applications
Chemical industry
Versatility
Industrial processes
Chemical structure
C10H14O2
Solubility
Solvent properties
Reactivity
Intermediate in synthesis
Physical state
Liquid or solid (depending on temperature)
Check Digit Verification of cas no
The CAS Registry Mumber 196871-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,8,7 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 196871-46:
(8*1)+(7*9)+(6*6)+(5*8)+(4*7)+(3*1)+(2*4)+(1*6)=192
192 % 10 = 2
So 196871-46-2 is a valid CAS Registry Number.
196871-46-2Relevant articles and documents
Regioselective bromomethylation of 1,2-dialkylbenzenes
Garg, Nupur,Lee, T. Randall
, p. 310 - 312 (2007/10/03)
This paper describes a systematic exploration of the regioselective bromomethylation of 1,2-dialkylbenzenes as a function of the reaction temperature and the chain length of the alkyl groups. At both 80 and 110 °C, bromomethyl groups can be introduced into the 4 and 5 positions of 1,2-dialkylbenzenes with high selectivity when the alkyl chains consist of two or more carbon atoms.
A Novel Cyclization of 1,2-Bis(2,2-dibromocyclopropyl)benzenes with Methyllithium
Hoehn, Juergen,Weyerstahl, Peter
, p. 808 - 814 (2007/10/02)
The CBr2 bis adducts 7, 8, and 10 react with MeLi at - 78 deg C to give the dicyclopropanaphthalenes 17 - 19.Thus, from meso-7 syn-17, and from d,l-7 anti-17 are formed stereoselectively.The reaction may proceed via the intermediates A or B.The carbenoid
