56671-72-8 Usage
Type of compound
Cycloalkane
It is a type of hydrocarbon with a ring of carbon atoms.
Structure
Cyclohexyl group attached to a hex-1-enyl group, which is attached to another cyclohexane ring
The compound has a complex structure with multiple ring structures connected to each other.
Physical state
Colorless liquid
It is a liquid at room temperature and is colorless in appearance.
Molecular weight
248.44 g/mol
The mass of one mole of the compound is 248.44 grams.
Industrial applications
Used in the manufacture of fragrances and flavorings
The compound is utilized in the production of various scented and flavored products.
Chemical intermediate
Used in the production of other organic compounds
It serves as a starting material or building block for synthesizing other organic molecules.
Solubility
Not specified in the material provided
The solubility of the compound in different solvents is not mentioned in the given information.
Boiling point
Not specified in the material provided
The temperature at which the compound transitions from a liquid to a gas is not provided.
Melting point
Not specified in the material provided
The temperature at which the compound transitions from a solid to a liquid is not mentioned in the given information.
Check Digit Verification of cas no
The CAS Registry Mumber 56671-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,7 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56671-72:
(7*5)+(6*6)+(5*6)+(4*7)+(3*1)+(2*7)+(1*2)=148
148 % 10 = 8
So 56671-72-8 is a valid CAS Registry Number.
56671-72-8Relevant academic research and scientific papers
Masuda, Yuzuru,Arase, Akira,Suzuki, Akira
, p. 1652 - 1655 (1980)
The reaction of (1-halo-1-alkenyl)dialkylboranes with lead(IV) acetate or (diacetoxyiodo)benzene was studied. (1-Bromo-1-alkenyl)dialkylboranes gave 1-bromo-1,2-dialkylethylenes.When alkyl groups on the boron atom of vinylboranes were bulky or the reaction temperatures were low, Z-isomers were afforded, whereas when alkyl groups on the boron atom were small or the reaction temperatures were relatively high, E-isomers were afforded as the main products. (1-Chloro-1-alkenyl)dialkylboranes gave (Z)-1-chloro-1,2-dialkylethylenes regardless of the reaction conditions. (1-Iodo-1-alkenyl)dialkylboranes failed to give satisfactory yields of 1-iodo-1,2-dialkylethylenes.
