94670-76-5 Usage
Chemical Structure
1,3-Benzodioxole, 5-bromo-6-iodo-
Derivative of Benzodioxole
Yes
Explanation
1,3-Benzodioxole, 5-bromo-6-iodois a derivative of the parent compound benzodioxole, which means it has a similar structure but with additional functional groups (in this case, bromine and iodine atoms).
Explanation
The compound contains both bromine and iodine atoms, which are halogens. These atoms can participate in various chemical reactions and contribute to the compound's unique properties.
Explanation
Due to its unique structure and properties, 1,3-Benzodioxole, 5-bromo-6-iodois used in various fields, including the synthesis of organic compounds, research in the pharmaceutical industry, and the production of industrial chemicals.
Explanation
The presence of bromine and iodine atoms in the compound allows it to be used as a building block for the creation of more complex chemical compounds, which can have a wide range of applications in different industries.
Explanation
The presence of both bromine and iodine atoms in the compound gives it unique properties, such as reactivity, stability, and solubility, which can be exploited in various chemical reactions and applications.
Presence of Halogen Atoms
Bromine and Iodine
Applications
Organic synthesis, pharmaceutical research, and industrial chemical production
Building Block for Complex Compounds
Yes
Unique Properties
Influenced by bromine and iodine atoms
Check Digit Verification of cas no
The CAS Registry Mumber 94670-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,6,7 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 94670-76:
(7*9)+(6*4)+(5*6)+(4*7)+(3*0)+(2*7)+(1*6)=165
165 % 10 = 5
So 94670-76-5 is a valid CAS Registry Number.
94670-76-5Relevant articles and documents
Asymmetric C–H activation as a modern strategy towards expedient synthesis of steganone
Dherbassy, Quentin,Wencel-Delord, Joanna,Colobert, Fran?oise
, p. 5238 - 5245 (2016)
A formal synthesis of (+)-steganone by means of atroposelective C–H activation is reported. The herein described strategy is very straightforward as the targeted scaffold is afforded in only 10 steps, amongst which five of them are conducted without isola
Fused Amino Pyridines for the Treatment of Lung Cancer
-
Paragraph 0149, (2016/11/17)
The present invention relates to the use of compounds with fused amino pyridine core for the treatment of malignancies associated with brain and lung. The oral administration of compounds of the instant application results in effective brain penetration and provides for non-intrusive treatment of brain and lung tumors.
Atropo-diastereoselective coupling of aryllithiums and arynes — variations around the chiral auxiliary
Augros, David,Yalcouye, Boubacar,Berthelot-Bréhier, Ana?s,Chessé, Matthieu,Choppin, Sabine,Panossian, Armen,Leroux, Frédéric R.
, p. 5208 - 5220 (2016/08/02)
The atropo-selective coupling of in situ generated arynes and aryllithiums bearing various chiral auxiliaries ortho to lithium (tert-butylsulfoxide, para-tolylsulfoxide, tartrate-derived chiral diethers and oxazolines) is described. Chiral oxazolines showed the best results in terms of yields of coupling products. Different reaction parameters like the nature of the aryne precursor, the oxazoline, the alkyllithium base or the solvent revealed to be crucial for obtaining good yields and for diastereoselection.
