76177-02-1 Usage
Uses
Used in Organic Synthesis:
(1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol 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 intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
(1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol is used as a precursor for the preparation of biologically active compounds. Its stereochemistry and chemical properties can be leveraged to develop new drugs with specific therapeutic effects. (1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol's potential as a building block allows for the exploration of novel drug candidates with improved efficacy and selectivity.
Used in Agrochemical Industry:
(1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol is used as a starting material for the development of agrochemicals, such as pesticides and herbicides. Its structural features can be utilized to create new molecules with enhanced activity against pests and weeds, contributing to more effective and sustainable agricultural practices.
Used in Specialty Chemicals:
(1R,2S)-2-methoxy-1,2-dihydroacenaphthylen-1-ol is used as a key component in the production of specialty chemicals, which have applications in various industries such as coatings, adhesives, and materials science. Its unique properties can be exploited to develop innovative products with improved performance characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 76177-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,7 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76177-02:
(7*7)+(6*6)+(5*1)+(4*7)+(3*7)+(2*0)+(1*2)=141
141 % 10 = 1
So 76177-02-1 is a valid CAS Registry Number.
76177-02-1Relevant articles and documents
1,2-DERIVATIVES OF ACENAPHTHYLENE. II. THERMAL STABILITY OF ACENAPHTHYLENE OXIDE AND ITS REACTION WITH ALCOHOLS
Anikin, V. F.,Levandovskaya, T. I.
, p. 1762 - 1766 (2007/10/02)
Acenaphthylene oxide can be obtained with a high yield from acenaphthylene chlorohydrin acetate.When heated above 130 deg C, it isomerizes to acenaphthenone.With alcohols and potassium hydroxide it is converted into E-1,2-dihydro-1-alkoxy-2-hydroxy derivatives of acenaphthylene.
Synthetic Photochemistry. XVIII. A Sensitizer Dependence in the Photooxidation of Indene and Acenaphthylene. The Occurrence of cis-1,2-Glycol Formation in a Rose Bengal-sensitized Reaction
Hatsui, Toshihide,Takeshita, Hitoshi
, p. 2655 - 2658 (2007/10/02)
Upon Rose Bengal-sensitized photooxygenation, indene and acenaphthylene afforded substantial amounts of the expected cis-glycols by means of the reduction of the intermediate dioxetanes.The formerly proposed structure of one of the isomeric methoxy hydroperoxides was revised on the basis of the chemical and spectral evidence.
