15753-47-6 Usage
Description
1-(Hydroxymethyl)cyclohexanol is a cyclohexane derivative with the molecular formula C7H14O2, featuring a hydroxymethyl substituent. It can exist in various isomers and is utilized as a versatile building block in organic synthesis.
Uses
Used in Pharmaceutical Industry:
1-(Hydroxymethyl)cyclohexanol serves as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Agrochemical Industry:
1-(hydroxymethyl)cyclohexanol is utilized in the production of agrochemicals, playing a crucial role in the creation of pesticides and other agricultural products to enhance crop protection and yield.
Used in Fine Chemicals Production:
1-(Hydroxymethyl)cyclohexanol is employed as a building block for the synthesis of fine chemicals, which are important in various specialized applications, including fragrances, dyes, and other high-value chemical products.
Used as a Solvent:
Due to its unique properties, 1-(hydroxymethyl)cyclohexanol can be used as a solvent in various chemical processes, aiding in the dissolution and reaction of other substances.
Used in Personal Care Product Formulation:
1-(hydroxymethyl)cyclohexanol finds application in the formulation of personal care products, such as cosmetics and toiletries, where it may contribute to the product's texture, stability, or effectiveness.
Used in Material Science and Polymer Development:
1-(Hydroxymethyl)cyclohexanol holds potential in the development of new materials and polymers, owing to its distinctive structural properties, which can be harnessed to create innovative and improved materials for various industries.
It is important to handle 1-(hydroxymethyl)cyclohexanol with care due to its potential health and safety risks if not managed properly.
Check Digit Verification of cas no
The CAS Registry Mumber 15753-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,5 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15753-47:
(7*1)+(6*5)+(5*7)+(4*5)+(3*3)+(2*4)+(1*7)=116
116 % 10 = 6
So 15753-47-6 is a valid CAS Registry Number.
15753-47-6Relevant articles and documents
N-(chloromethyloxycarbonyl)pyrrolidine as a source of the HOCH2- synthon
Guijarro, Albert,Yus, Miguel
, p. 5593 - 5596 (1996)
The reaction of N-(chloromethyloxycarbonyl)pyrrolidine (1) with lithium powder and a catalytic amount of DTBB (2.5 mol %) in the presence of different electrophiles [Me3SiCl, Bu(i)CHO, Bu(t)CHO, PhCHO, Et2CO, (CH2)5CO, PhCOMe, Ph2CO] in THF at -78°C leads, after hydrolysis with water, to the expected functionalised carbamates 2. Deprotection of the acetophenone derivative 2g with DIBALH at THF reflux yields, after hydrolysis, the corresponding 1,2-diol 3g.
Selective transition-metal-free vicinal cis-dihydroxylation of saturated hydrocarbons
Bering, Luis,Antonchick, Andrey P.
, p. 452 - 457 (2016/12/30)
A transition-metal-free cis-dihydroxylation of saturated hydrocarbons under ambient reaction conditions has been developed. The described approach allows a direct and selective synthesis of vicinal diols. The new reaction thereby proceeds via radical iodination and a sequence of oxidation steps. A broad scope of one-pot dual C(sp3)-H bond functionalization for the selective synthesis of vicinal syn-diols was demonstrated.
Mild deprotection of methylene acetals in combination with trimethylsilyl triflate-2,2′-bipyridyl
Fujioka, Hiromichi,Senami, Kento,Kubo, Ozora,Yahata, Kenzo,Minamitsuji, Yutaka,Maegawa, Tomohiro
experimental part, p. 426 - 428 (2011/02/26)
The facile deprotection of methylene acetal protection of diols under mild conditions is established. The combination of trimethylsilyl triflate (TMSOTf) and 2,2′-bipyridyl followed by a weakly acidic hydrolysis was effective and the substrates having acid sensitive functional groups can be tolerated under the stated conditions. The selective deprotection between methylene acetal and benzophenone ketal was achieved.
