70786-44-6 Usage
Uses
Used in Pharmaceutical Industry:
Benzofuran, 2,3,3a,4,5,7a-hexahydro-3,6-dimethylis used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, Benzofuran, 2,3,3a,4,5,7a-hexahydro-3,6-dimethylis employed as a precursor in the production of agrochemicals, aiding in the creation of compounds that can enhance crop protection and yield.
Used in Organic Compounds Synthesis:
Benzofuran, 2,3,3a,4,5,7a-hexahydro-3,6-dimethylis utilized as a building block in the synthesis of a range of organic compounds, providing a structural foundation for the development of novel chemical entities with diverse applications.
Used in Research and Development:
Benzofuran, 2,3,3a,4,5,7a-hexahydro-3,6-dimethylis also used in research and development within the chemical and pharmaceutical industries, where it serves as a valuable tool for exploring new chemical reactions and pathways, potentially leading to breakthroughs in material and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 70786-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,8 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70786-44:
(7*7)+(6*0)+(5*7)+(4*8)+(3*6)+(2*4)+(1*4)=146
146 % 10 = 6
So 70786-44-6 is a valid CAS Registry Number.
70786-44-6Relevant academic research and scientific papers
Chemical Tranformation of Terpenoids. V. Acidic Conversions of 10-Hydroxygeraniol and 10-Hydroxynerol Derivatives Leading to Cyclic Monoterpenoids
Kitagawa, Isao,Tsujii, Shinji,Nishikawa, Fumiko,Shibuya, Hirotaka
, p. 2639 - 2651 (2007/10/02)
Acid treatment of 1-O-acetyl-10-hydroxygeraniol (5a), 1-O-methyl-10-hydroxygeraniol (5b), 1-O-acetyl-10-hydroxynerol (6a), and 1-O-methyl-10-hydroxynerol (6b) was investigated under various conditions.It was found that treatment of 5a and 6a with HCOOH gave menth-1-ene-8,9-diol (7), while treatment of 5a, 5b, 6a, or 6b with BF3-etherate in CH2Cl2 furnished two menthofuran-type compounds (9, 10) and two bicyclooct-2-ene derivatives (17, 24).Both 9 and 10 were successfully converted to menthofuran (16) and 17 was converted to a bicyclooctenone derivative (23) which was a key intermediate for a synthesis of juvabione (27).Keywords - geraniol; nerol; 10-hydroxygeraniol; 10-hydroxynerol; 10-hydroxygeraniol derivative; 10-hydroxynerol derivative; uroterpenol; menthofuran; bicyclooct-2-ene derivative