112778-17-3 Usage
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), and oxygen (O) atoms in a molecule of 1,4-Heptanediol, 7-(3-methoxyphenyl)-.
Explanation
1,4-Heptanediol, 7-(3-methoxyphenyl)is a derivative of heptanediol, which is a type of alcohol compound.
Explanation
This group refers to a benzene ring with a methoxy (CH3O-) substituent attached to the 7th carbon of the heptanediol chain.
Explanation
1,4-Heptanediol, 7-(3-methoxyphenyl)can be used in various applications, including the production of pharmaceuticals, fragrances, and other fine chemicals.
Explanation
The compound may also have potential uses as a precursor in organic synthesis or as a building block for more complex molecules.
Explanation
As with any chemical compound, it is important to handle 1,4-Heptanediol, 7-(3-methoxyphenyl)with caution and in accordance with safety guidelines to prevent accidents or health hazards.
Type of Compound
Alcohol derivative
Substituent
7-(3-methoxyphenyl)-
Applications
Pharmaceutical production, fragrances, and fine chemicals
Potential Uses
Precursor in organic synthesis, building block for complex molecules
Safety Precautions
Handle with caution, follow safety guidelines
Check Digit Verification of cas no
The CAS Registry Mumber 112778-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,7 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 112778-17:
(8*1)+(7*1)+(6*2)+(5*7)+(4*7)+(3*8)+(2*1)+(1*7)=123
123 % 10 = 3
So 112778-17-3 is a valid CAS Registry Number.
112778-17-3Relevant academic research and scientific papers
Maskill, H.
, p. 1739 - 1742 (1987)
The previously unknown methoxy substituted benzene derivative 2,3,3a,4,5,6-hexahydro-8-methoxy-1H-phenalene (3a) has been prepared by two routes.One starts from 6-methoxy-α-tetralone (4a) and involves a single 3-carbon extension and cycization of the alcohol (7b); the other starts from 3-(3-methoxyphenyl)propanoic acid (5a) and proceeds via a 4-carbon extension and a double cyclization of the diol (10).
