5830-14-8 Usage
Chemical structure
Cyclohexane ring with two hydroxyl groups and a hydroxymethyl group
Explanation
The compound has a six-membered carbon ring (cyclohexane) with two hydroxyl (OH) groups and a hydroxymethyl (CH2OH) group attached to it.
Explanation
A diol is a type of alcohol that contains two hydroxyl (OH) groups. In 1,2-Cyclohexanediol, 1-(hydroxymethyl)-, the two hydroxyl groups are attached to the cyclohexane ring.
Explanation
Due to its unique structure, 1,2-Cyclohexanediol, 1-(hydroxymethyl)can be used as a starting material or intermediate in the production of various organic compounds.
Explanation
The compound has been identified as a potential ingredient in the formulation of cosmetic and personal care products, likely due to its low toxicity and compatibility with other ingredients.
Explanation
1,2-Cyclohexanediol, 1-(hydroxymethyl)is considered to have low toxicity, making it relatively safe for use in commercial and industrial settings.
Explanation
Given its low toxicity, the compound is deemed suitable for use in various applications without posing significant health or environmental risks.
Classification
Diol
Industrial applications
Building block in the synthesis of other organic compounds
Potential use
Ingredient in cosmetic and personal care products
Toxicity
Low toxicity
Safety
Relatively safe for commercial and industrial use
Check Digit Verification of cas no
The CAS Registry Mumber 5830-14-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5830-14:
(6*5)+(5*8)+(4*3)+(3*0)+(2*1)+(1*4)=88
88 % 10 = 8
So 5830-14-8 is a valid CAS Registry Number.
5830-14-8Relevant academic research and scientific papers
Herbicidal 1,3-dioxanes
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, (2008/06/13)
A new class of herbicidal compounds consisting of 1,3-dioxanes carrying substituents other than hydrogen in the 2-, 4-, 5-, and 6-positions of the dioxane ring exhibits preemergence and postemergence herbicidal activity, controlling effectively the growth of selected grassy species. The synthesis of members of this class is described in detail, and the utility of representative compounds is exemplified.
