35970-34-4 Usage
Uses
Used in Organic Synthesis:
2-BROMO-1-(3,4-DIHYDRO-2H-1,5-BENZODIOXEPIN-7-YL)ETHAN-1-ONE is used as a key intermediate in organic synthesis for the creation of various chemical compounds. Its unique structure allows it to participate in a range of chemical reactions, facilitating the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-BROMO-1-(3,4-DIHYDRO-2H-1,5-BENZODIOXEPIN-7-YL)ETHAN-1-ONE is used as a starting material or a building block in the development of new pharmaceuticals. Its potential applications may include the creation of novel drug candidates, particularly those targeting specific biological pathways or receptors.
Safety Considerations:
It is crucial to handle 2-BROMO-1-(3,4-DIHYDRO-2H-1,5-BENZODIOXEPIN-7-YL)ETHAN-1-ONE with care and adhere to all necessary safety protocols when working with this chemical. Proper handling minimizes risks associated with chemical exposure and ensures the safety of researchers and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 35970-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,7 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35970-34:
(7*3)+(6*5)+(5*9)+(4*7)+(3*0)+(2*3)+(1*4)=134
134 % 10 = 4
So 35970-34-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H11BrO3/c12-7-9(13)8-2-3-10-11(6-8)15-5-1-4-14-10/h2-3,6H,1,4-5,7H2
35970-34-4Relevant academic research and scientific papers
An efficient strategy for protecting dihydroxyl groups of catechols
Huang, Wei-Bin,Guo, Ying,Jiang, Jian-An,Pan, Xian-Dao,Liao, Dao-Hua,Ji, Ya-Fei
, p. 741 - 746 (2013/05/09)
A novel strategy for protecting dihydroxyl groups of catechols has been developed. Base-mediated cyclizations of catechols with 1,3-dibromopropane provided the corresponding benzo[b]1,4-dioxepans, and herefrom the protecting group was easily cleaved by aluminum chloride. The preparation of the antibacterial and antifungal agent 4-(2-aminothiazol-4-yl)benzene-1,2-diol from catechol reliably verified its availability amenable to various harsh reaction conditions. Georg Thieme Verlag Stuttgart - New York.
