728878-73-7 Usage
Explanation
The compound is composed of 8 carbon atoms, 14 hydrogen atoms, and 2 oxygen atoms.
Explanation
It is derived from cycloheptanediol, which is a seven-membered ring with two hydroxyl groups.
Explanation
The compound contains a methyl (CH3) group and a methylene (CH2) group attached to the cycloheptane ring.
Explanation
The compound exists as a mixture of different stereoisomers, which are molecules with the same molecular formula but different spatial arrangements of atoms.
Explanation
This particular compound has a (1R,2R)-relconfiguration, which refers to the specific arrangement of the methyl and methylene groups in the molecule.
Explanation
The exact properties and uses of the compound may differ based on the specific stereoisomer and the intended application, such as its reactivity, solubility, or stability.
Explanation
The 9CI is a unique identifier assigned to the compound by the Chemical Abstracts Service, which is a registry of chemical substances.
Structure
Cycloheptanediol derivative
Substituents
Methyl and methylene groups
Stereoisomers
Mixture of stereoisomers
Specific Configuration
(1R,2R)-rel-
Applications
Organic synthesis and pharmaceutical industry
Properties
Vary depending on stereoisomer and application
Chemical Abstracts Service (CAS) Registry Number
9CI
Check Digit Verification of cas no
The CAS Registry Mumber 728878-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,8,8,7 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 728878-73:
(8*7)+(7*2)+(6*8)+(5*8)+(4*7)+(3*8)+(2*7)+(1*3)=227
227 % 10 = 7
So 728878-73-7 is a valid CAS Registry Number.
728878-73-7Relevant academic research and scientific papers
Intramolecular chromium(II)-catalyzed pinacol cross coupling of 2-methylene-α,ω-dicarbonyls
Groth, Ulrich,Jung, Marc,Vogel, Till
, p. 1054 - 1058 (2007/10/03)
Using only 10% of CrCl2 as catalyst, manganese-powder as reducing agent and TMSC1 as scavenger, 2-methylene-α,ω-dialdehydes and -ketones can be coupled to form cyclic diols diastereoselectively. The diastereomeric excess strongly depends on the ring size and the substituents of the ω-carbonyl group. The greater the ring size the higher diastereoselectivities are observed. In all cases cis-diols are preferentially formed.
