36400-98-3 Usage
Uses
Used in Pharmaceutical Industry:
2-(4,4-dimethylpentan-2-yl)-5,7,7-trimethyl-octan-1-ol is used as a reagent for the synthesis of new ascorbic acid derivatives, which may possess pro-vitamin C properties. These derivatives are valuable in the development of pharmaceutical formulations, particularly those aimed at promoting skin health and providing antioxidant benefits.
Used in Cosmetics Industry:
In the cosmetics industry, 2-(4,4-dimethylpentan-2-yl)-5,7,7-trimethyl-octan-1-ol is utilized as a key ingredient in the formulation of skin-care products. Its role as a precursor to pro-vitamin C derivatives makes it an essential component in products designed to improve skin texture, reduce the appearance of aging, and provide overall skin nourishment.
Used in Chemical Research:
2-(4,4-dimethylpentan-2-yl)-5,7,7-trimethyl-octan-1-ol also serves as a valuable compound in chemical research, particularly in the study of organic synthesis and the development of novel chemical reactions. Its unique structure and reactivity make it an interesting subject for exploration and potential application in various chemical processes.
Overall, 2-(4,4-dimethylpentan-2-yl)-5,7,7-trimethyl-octan-1-ol is a versatile compound with a range of applications across different industries, primarily due to its role in the synthesis of pro-vitamin C derivatives and its potential for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 36400-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,4,0 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36400-98:
(7*3)+(6*6)+(5*4)+(4*0)+(3*0)+(2*9)+(1*8)=103
103 % 10 = 3
So 36400-98-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H38O/c1-14(11-17(3,4)5)9-10-16(13-19)15(2)12-18(6,7)8/h14-16,19H,9-13H2,1-8H3
36400-98-3Relevant academic research and scientific papers
Quinoid-Aromatic Resonance for Very Small Optical Energy Gaps in Small-Molecule Organic Semiconductors: A Naphthodithiophenedione-oligothiophene Triad System
Kawabata, Kohsuke,Takimiya, Kazuo
supporting information, p. 15660 - 15670 (2021/10/12)
Organic semiconductors with very small optical energy gaps have attracted a lot of attention for near-infrared-active optoelectronic applications. Herein, we present a series of donor-acceptor-donor (D?A?D) organic semiconductors consisting of a highly electron-deficient naphtho[1,2-b:5,6-b′]dithiophene-2,7-dione quinoidal acceptor and oligothiophene donors that show very small optical energy gaps of down to 0.72 eV in the solid state. Investigation of the physicochemical properties of the D?A?D molecules as well as theoretical calculations of their electronic structures revealed an efficient intramolecular interaction between the quinoidal acceptor and the aromatic oligothiophene donors in the D?A?D molecules; this significantly enhances the backbone resonance and thus reduces the bond length alternation along the π-conjugated backbones. Despite the very small optical energy gaps, the D?A?D molecules have low-lying frontier orbital energy levels that give rise to air-stable ambipolar carrier transport properties with hole and electron mobilities of up to 0.026 and 0.043 cm2 V?1 s?1, respectively, in field-effect transistors.
Method for preparing branched alcohol
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Page/Page column 6; 7; 8, (2019/01/25)
A method for preparing a branched alcohol by dimerizing an aliphatic monoalcohol having three or more carbon atoms in the presence of a base and a catalyst. The dimerization reaction is performed under atmospheric pressure while injecting a hydrogen gas. With this method, it is possible to obtain a dimerized alcohol with excellent yield even when using a branched aliphatic monoalcohol as the starting material.
