58851-64-2 Usage
Description
1a,2,7,7a-Tetrahydro-3,6-diMethoxy-naphth[2,3-b]oxirene is a complex organic compound characterized by its unique molecular structure, which includes a naphthalene core with an oxirene (epoxide) ring fused to it. The molecule also features two methoxy groups at positions 3 and 6, and a tetrahydro ring system at positions 1a and 7a. 1a,2,7,7a-Tetrahydro-3,6-diMethoxy-naphth[2,3-b]oxirene is known for its potential applications in various fields due to its chemical properties.
Uses
1. Used in Pharmaceutical Industry:
1a,2,7,7a-Tetrahydro-3,6-diMethoxy-naphth[2,3-b]oxirene is used as a leukotriene inhibitor for its ability to block the action of leukotrienes, which are inflammatory mediators involved in various diseases, including asthma and other respiratory conditions. By inhibiting leukotrienes, this compound can help reduce inflammation and alleviate symptoms associated with these conditions.
2. Used in Chemical Research:
1a,2,7,7a-Tetrahydro-3,6-diMethoxy-naphth[2,3-b]oxirene can also be utilized in chemical research as a starting material or intermediate for the synthesis of other complex organic molecules. Its unique structure and functional groups make it a valuable building block for the development of new compounds with potential applications in various industries, such as pharmaceuticals, agrochemicals, and materials science.
3. Used in Material Science:
Due to its structural features, 1a,2,7,7a-Tetrahydro-3,6-diMethoxy-naphth[2,3-b]oxirene may find applications in the development of novel materials with specific properties, such as improved stability, enhanced reactivity, or unique optical characteristics. These materials could be used in various applications, including coatings, adhesives, or advanced composites.
Check Digit Verification of cas no
The CAS Registry Mumber 58851-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,5 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58851-64:
(7*5)+(6*8)+(5*8)+(4*5)+(3*1)+(2*6)+(1*4)=162
162 % 10 = 2
So 58851-64-2 is a valid CAS Registry Number.
58851-64-2Relevant articles and documents
Synthesis of anthracyclinone precursor: 5,12-dihydroxy-1,3,4- trihydronaphthacene-2,6,11-quinone
Tririya, Gasirat,Zanger, Murray
, p. 3047 - 3059 (2007/10/03)
Two practical and efficient approaches for preparing large quantities of 5,12-dihydroxy-1,3,4-trihydronaphthacene-2,6,11-quinone 9 are described. Both synthetic approaches involve a simple route with a fewer number of steps and utilize readily available and inexpensive starting materials. Large-scale production of this precursor may prove to be useful for further research involving the synthesis of antineoplastic anthracyclines and development of their analogs with increased activity and decreased toxicity.
P-aminophenols, derivatives thereof and method of use
-
, (2008/06/13)
p-Aminophenols are provided having the structure STR1 wherein m is 0, 1 or 2; n is 0, 1, 2 or 3; R1 and R2 may be the same or different and are H, hydroxy or alkoxy; R3 is H, lower alkyl, alkanoyl or aroyl and R4 is H, lower alkyl or alkanoyl, and including acid-addition salts thereof. These compounds are useful as inhibitors of leukotriene production and as such are useful as antiallergy, anti-inflammatory and anti-psoriatic agents.
A novel racemization mechanism for the α-hydroxy ketone moiety(C9-position) of optically active anthracyclinone derivatives
Terashima,Tamoto
, p. 2589 - 2592 (2007/10/02)
The facile acid-catalyzed racemization of optically active anthracyclinone derivatives((S)(+)-1a,b) was found to proceed through the ring-expanded seven-membered α-hydroxyketones(2 and/or 3 for (S)(+)-1a) by subjecting various plausible intermediates to t
