100858-26-2 Usage
Uses
Used in Organic Synthesis:
(1R,3aR,7aR)-1-((2R,5S,E)-6-(MethoxyMethoxy)-5,6-diMethylhept-3-en-2-yl)-7a-Methylhexahydro-1H-inden-4(2H)-one is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure and functional groups make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (1R,3aR,7aR)-1-((2R,5S,E)-6-(MethoxyMethoxy)-5,6-diMethylhept-3-en-2-yl)-7a-Methylhexahydro-1H-inden-4(2H)-one is used as an intermediate in the synthesis of novel drug candidates. Its diverse functional groups and complex structure allow for the development of innovative therapeutic agents with unique mechanisms of action.
Used in Agrochemical Industry:
(1R,3aR,7aR)-1-((2R,5S,E)-6-(MethoxyMethoxy)-5,6-diMethylhept-3-en-2-yl)-7a-Methylhexahydro-1H-inden-4(2H)-one is utilized as a key component in the development of new agrochemicals, such as pesticides and herbicides. Its structural complexity and functional groups enable the creation of effective and targeted crop protection products.
Used in Specialty Chemicals:
In the specialty chemicals sector, (1R,3aR,7aR)-1-((2R,5S,E)-6-(MethoxyMethoxy)-5,6-diMethylhept-3-en-2-yl)-7a-Methylhexahydro-1H-inden-4(2H)-one is employed as a precursor for the synthesis of high-value specialty chemicals. Its unique properties and reactivity make it suitable for applications in various industries, such as materials science, fragrances, and dyes.
Check Digit Verification of cas no
The CAS Registry Mumber 100858-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,5 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100858-26:
(8*1)+(7*0)+(6*0)+(5*8)+(4*5)+(3*8)+(2*2)+(1*6)=102
102 % 10 = 2
So 100858-26-2 is a valid CAS Registry Number.
100858-26-2Relevant articles and documents
PROCESS FOR PRODUCTION OF INDENE DERIVATIVE, AND INTERMEDIATE FOR PRODUCTION OF THE DERIVATIVE
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Page/Page column 15; 16, (2009/01/24)
Indene derivatives that are utilizable as intermediates in the synthesis of the vitamin D2 derivative paricalcitol, which is useful as pharmaceutical are efficiently prepared by subjecting a vitamin D2 derivative such as 25-hydroxyvi
25-Hydroxydihydrotachysterol2. An innovative synthesis of a key metabolite of dihydrotachysterol2
Hanekamp,Rookhuizen,Bos,Brandsma
, p. 9283 - 9294 (2007/10/02)
A new synthesis of 25-hydroxydihydrotachysterol2 is described. The hydroxylated side-chain is constructed stereoselectively using a chiral Wittig reagent. The A-ring synthon is introduced utilising the Wittig-Horner method as developed by Lythgoe et al. The preparation of the metabolite is carried out in 18 steps.
Studies on the Synthesis of Side-Chain Hydroxylated Metabolites of Vitamin D. 2. Stereocontrolled Synthesis of 25-Hydroxyvitamin D2
Sardina, F. Javier,Mourino, Antonio,Castedo, Luis
, p. 1264 - 1269 (2007/10/02)
An efficient synthesis of 25-hydroxyvitamin D2 is described.The chiral center at C-24 was introduced by the stereospecific and regioselective displacement of an allylic carbamate by a cuprate.The triene system was assembled by Horner-Wittig coupling of ke
