1438-55-7 Usage
Description
(1S,βS)-1,4,4aα,5,6,7,8,8a-Octahydro-β,2,5,5,8aβ-pentamethyl-1β-naphthalenepentanoic acid methyl ester is a complex organic compound characterized by a naphthalene ring and multiple methyl groups. As a methyl ester of a carboxylic acid, it possesses a diverse range of structural features that may contribute to its potential biological activity and applications in various fields.
Uses
Used in Organic Synthesis:
(1S,βS)-1,4,4aα,5,6,7,8,8a-Octahydro-β,2,5,5,8aβ-pentamethyl-1β-naphthalenepentanoic acid methyl ester is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows it to be a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Applications:
Due to its complex structure and the presence of a naphthalene ring, (1S,βS)-1,4,4aα,5,6,7,8,8a-Octahydro-β,2,5,5,8aβ-pentamethyl-1β-naphthalenepentanoic acid methyl ester may have potential pharmaceutical applications. Further research and investigation would be required to explore its biological activity and potential use as a drug candidate or in the development of drug delivery systems.
Used in Chemical Research:
(1S,βS)-1,4,4aα,5,6,7,8,8a-Octahydro-β,2,5,5,8aβ-pentamethyl-1β-naphthalenepentanoic acid methyl ester can be utilized in chemical research to study the effects of its structural features on various chemical and biological properties. This may include investigations into its reactivity, stability, and interactions with other molecules, which could lead to new insights and applications in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1438-55-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,3 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1438-55:
(6*1)+(5*4)+(4*3)+(3*8)+(2*5)+(1*5)=77
77 % 10 = 7
So 1438-55-7 is a valid CAS Registry Number.
1438-55-7Relevant articles and documents
3α-ANGELOYLOXY-2α-HYDROXYCATIVIC ACID, A NEW DITERPENE FROM BRICKELLIA PANICULATA
Gomez, F.,Quijano, L.,Calderon, J. S.,Rios, T.
, p. 1292 - 1293 (1983)
The investigation of Brickellia paniculata resulted in the isolation of a new diterpene of the labdane type.It was identified as 3α-angeloyloxy-2α-hydroxycativic acid by chemical and spectroscopic methods. - Key Word Index: Brickellia paniculata; Compositae; diterpene; 3α-angeloyloxy-2α-hydroxycativic acid.
Cell growth activating composition containing compound having labdane structure
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Page column 6, (2008/06/13)
The present invention provides compounds which have, particularly, an inhibitory activity on production of melanin, a cell activating activity and an anti-bacterial activity, are derived from natural sources, and are safe and not harmful. One or more compounds represented by the following general formula are contained: wherein R1represents —CH2OH, —COOR6or —COOX, whereupon X is a group capable forming a salt and R6represents hydrogen or a C1to C3lower alkyl group; R2to R5each represent hydrogen or a methyl group; and . . . A . . . represents ═C(CH3)—, —C(CH3)═, —C(═CH2)—, —CH(CH3)— or —C(OH)(CH3)—.
REACTIVITY OF METHYL LABDANOLATE WITH LEAD TETRAACETATE
Pascual Teresa, J. de,Urones, J. G.,Montana Pedrero, A.,Basabe Barcala, P.
, p. 4563 - 4576 (2007/10/02)
The reactivity of the methyl labdanolate, 3 with Pb(OAc)4 and/or Pb(OAc)4/I2 was studied.The long distance functionalization at C-12 led to compounds 8b and 9b, whose oxidation with RuO4 produced 16 at a 100percent yield.Compounds 14 and 15 were obtained
