472-92-4 Usage
Description
3,7,12,16,20,24-Hexamethyl-1-[(1R)-2,6,6-trimethyl-1-cyclohex-2-enyl]pentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaene is a complex organic compound characterized by its long carbon chain and multiple methyl groups. It is derived from a pentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaene backbone with various methyl groups and a cyclohex-2-enyl group attached. 3,7,12,16,20,24-hexamethyl-1-[(1R)-2,6,6-trimethyl-1-cyclohex-2-enyl]pentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaene is likely to have unique chemical and physical properties due to its structure.
Uses
Used in Pharmaceutical Industry:
3,7,12,16,20,24-Hexamethyl-1-[(1R)-2,6,6-trimethyl-1-cyclohex-2-enyl]pentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaene is used as a potential pharmaceutical compound for its unique chemical structure, which may offer specific interactions with biological targets or serve as a precursor for the synthesis of other bioactive molecules.
Used in Cosmetics Industry:
In the cosmetics industry, this compound may be used as an ingredient in various formulations due to its potential to improve the texture, stability, or performance of the final product. Its long-chain structure and hydrophobic nature could contribute to the moisturizing, emollient, or film-forming properties of cosmetics.
Used in Chemical Research:
3,7,12,16,20,24-Hexamethyl-1-[(1R)-2,6,6-trimethyl-1-cyclohex-2-enyl]pentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaene can be used in chemical research as a model compound for studying the effects of structural modifications on the properties and reactivity of organic molecules. It may also be used in the development of new synthetic methods or as a reference compound for analytical techniques.
Used in Material Science:
The unique structure of this compound may also find applications in material science, where it could be used to develop new materials with specific properties, such as improved thermal stability, mechanical strength, or chemical resistance.
Purification Methods
δ-Carotene crystallises from CS2/hexane/EtOH as red needles. The racemic carotene is purified through an alumina (Grade II) column by elution with 15% *C6H6/pet ether (b 60-80o), and the main band eluent is evaporated and the residue is crystallised from MeOH/pet ether (b 60-80o) to give -carotene with m 150-151o. [Porter & Anderson Arch Biochem 32 211951, Synthesis: Manchand et al. J Chem Soc 2019 1965, Absolute Config: Buchecher & Eugster Helv Chim Acta 54 327 1971, 5 III 2453, 5 IV 2617.] -Carotene (
Check Digit Verification of cas no
The CAS Registry Mumber 472-92-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 472-92:
(5*4)+(4*7)+(3*2)+(2*9)+(1*2)=74
74 % 10 = 4
So 472-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C40H56/c1-32(2)18-13-21-35(5)24-15-26-36(6)25-14-22-33(3)19-11-12-20-34(4)23-16-27-37(7)29-30-39-38(8)28-17-31-40(39,9)10/h11-12,14-16,18-20,22-30,39H,13,17,21,31H2,1-10H3/b12-11+,22-14+,23-16+,26-15+,30-29+,33-19+,34-20+,35-24+,36-25+,37-27+
472-92-4Relevant articles and documents
Synthesen von Carotinen mit ψ-Endgruppen und (Z)-Konfiguration an terminalen konjugierten Doppelbindungen
Zumbrunn, Albrecht,Uebelhart, Peter,Eugster, Conrad Hans
, p. 1519 - 1539 (2007/10/02)
Five carotenes bearing (5Z)-ψ-end groups were synthesized and carefully characterized: (5Z)-lycopene (6), (5Z,5'Z)-lycopene (7), (5'Z)-neurosporene (8), (5'Z)-β,ψ-carotene (12), and (5'Z)-εψ-carotene (14).
