6976-27-8 Usage
Description
(1,2-DIMETHYLPROPYL)CYCLOPROPANE, with the molecular formula C8H16, is a cycloalkane derivative characterized by a cyclopropane ring attached to a (1,2-dimethylpropyl) group. This chemical compound is a significant component in the realm of organic chemistry, particularly for the synthesis of more complex molecules and the study of cyclopropane chemistry.
Uses
Used in Organic Chemistry:
(1,2-DIMETHYLPROPYL)CYCLOPROPANE is used as a building block for the synthesis of more complex molecules, contributing to the development of advanced chemical compounds and materials.
Used in Cyclopropane Chemistry Research:
It serves as a subject of study for understanding the reactivity and behavior of cyclopropane compounds, which is crucial for advancing knowledge in the field of organic chemistry.
Used in Industrial and Pharmaceutical Applications:
While further research and testing are required, (1,2-DIMETHYLPROPYL)CYCLOPROPANE may have potential applications in various industries and pharmaceuticals, given its unique structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 6976-27-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6976-27:
(6*6)+(5*9)+(4*7)+(3*6)+(2*2)+(1*7)=138
138 % 10 = 8
So 6976-27-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H16/c1-6(2)7(3)8-4-5-8/h6-8H,4-5H2,1-3H3
6976-27-8Relevant articles and documents
HOMOALLYLIC SUBSTITUTION REACTIONS OF LITHIUM DIALKYL CUPRATES WITH CYCLOPROPYLCARBINYL HALIDES: MECHANISTIC CONSIDERATIONS
Hrubiec, Robert T.,Smith, Michael B.
, p. 1457 - 1468 (2007/10/02)
Highly reactive lithium dialkyl cuprates and 1-bromo-1-cyclopropylalkanes, 4, react to give good yields of the homoallylic substitution product, 6.Less reactive organocuprates react with 4 to give mixtures of 6 and the direct substitution product 7.These results are consistent with a copper(I) radical intermediate which undergoes facile rearrangement prior to reductive coupling.
