506-52-5 Usage
Description
1-Hexacosanol is a long-chain primary fatty alcohol that is hexacosane in which a hydrogen attached to one of the terminal carbons is replaced by a hydroxy group. It is characterized by its white powder appearance.
Uses
1. Used in Pharmaceutical Applications:
1-Hexacosanol is used as a therapeutic agent for reducing Parkinson's symptoms, as it has shown potential in contributing to the modulation of the release of proinflammatory mediators.
2. Used in Anti-Inflammatory Applications:
1-Hexacosanol is used as an anti-inflammatory agent, as it contributes to the modulation of the release of proinflammatory mediators, potentially providing relief from inflammation-related conditions.
3. Used in Cosmetics Industry:
1-Hexacosanol is used as an ingredient in the cosmetics industry, due to its long-chain primary fatty alcohol structure, which can provide moisturizing and emollient properties to various cosmetic products.
4. Used in Chemical Research:
1-Hexacosanol is used as a research compound in the field of organic chemistry, particularly for studying the properties and reactions of long-chain primary alcohols and their derivatives.
Check Digit Verification of cas no
The CAS Registry Mumber 506-52-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 506-52:
(5*5)+(4*0)+(3*6)+(2*5)+(1*2)=55
55 % 10 = 5
So 506-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C29H58O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-29(32)33-27-28(31)26-30/h28,30-31H,2-27H2,1H3/t28-/m0/s1
506-52-5Relevant articles and documents
Rowe et al.
, p. 235,236, 239 (1969)
PROCESS FOR THE PREPARATION OF ALIPHATIC PRIMARY ALCOHOLS AND RELATED INTERMEDIATES IN SUCH PROCESS
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Page/Page column 8, (2010/02/11)
The invention relates to protected alcohol with formula (R1 - O-)mPG, wherein R1 represents a linear, straight-chain alkyl group having 26-30 C-atoms, m is 1 or 2, and PG, forming an ether group in combination with the -O- of the former primary alcohol, represents a protecting group chosen from the group of substituted methyl, substituted ethyl, substituted benzyl and (substituted) silyl groups with at least one substituent on the Si-atom being not a methyl group, in case m = 1; and a diol protecting group in case m = 2, with the proviso that PG is no saccharide. The invention further relates to process for the preparation of such protected alcohols via an organometallic cross coupling reaction.
A New Synthesis of Long Chain Acid Esters and Carbinols
Rao, S. Jagadishwar,Bhalerao, U. T.,Tilak, B. D.
, p. 208 - 211 (2007/10/02)
A versatile synthesis of difficulty accessible long chain acid esters and carbinols is described.The synthesis involves acylations at 2- and 5-positions of thiophene.Thioketalation of the resulting ketoesters followed by Raney nickel desulfurization yield acid esters which on LAH reduction give the corresponding carbinols.
