100207-07-6 Usage
Explanation
The chemical formula for 1,2-Pentadiene, 1-bromo-4,4-dimethyl is C9H15Br, indicating the presence of 9 carbon atoms, 15 hydrogen atoms, and 1 bromine atom.
Explanation
The compound appears as a colorless liquid, which means it does not have a color and flows like a liquid at room temperature.
Explanation
1,2-Pentadiene, 1-bromo-4,4-dimethyl has a strong, pleasant smell that can be detected easily.
Explanation
1,2-Pentadiene, 1-bromo-4,4-dimethyl- is mainly used as an intermediate in the production of other chemicals, such as pharmaceuticals and pesticides.
Explanation
1,2-Pentadiene, 1-bromo-4,4-dimethyl is also utilized in the manufacturing of plastics and rubber products due to its chemical properties.
Explanation
The compound is considered to have mild toxicity, which means it can cause health issues if not handled properly.
Explanation
Exposure to 1,2-Pentadiene, 1-bromo-4,4-dimethyl may result in skin and eye irritation, as well as respiratory tract irritation if inhaled.
Explanation
To minimize the risk of health hazards, it is essential to handle 1,2-Pentadiene, 1-bromo-4,4-dimethyl with care and follow appropriate safety guidelines.
Physical state
Colorless liquid
Odor
Powerful, sweet
Primary use
Intermediate in chemical production
Industrial applications
Plastics and rubber products
Toxicity
Mildly toxic
Health hazards
Skin and eye irritation, respiratory tract irritation
Safety precautions
Handle with care, follow proper guidelines
Check Digit Verification of cas no
The CAS Registry Mumber 100207-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,0 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 100207-07:
(8*1)+(7*0)+(6*0)+(5*2)+(4*0)+(3*7)+(2*0)+(1*7)=46
46 % 10 = 6
So 100207-07-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H11Br/c1-7(2,3)5-4-6-8/h5-6H,1-3H3
100207-07-6Relevant academic research and scientific papers
Stereoretentive suzuki-miyaura coupling of haloallenes enables fully stereocontrolled access to (-)-Peridinin
Woerly, Eric M.,Cherney, Alan H.,Davis, Erin K.,Burke, Martin D.
supporting information; experimental part, p. 6941 - 6943 (2010/08/06)
Stimulated by the substantial challenge of synthesizing the complex and sensitive stereogenic allene-containing core of (-)-peridinin, the first stereocontrolled coupling of haloallenes with boronic acids has been achieved. This new method and the principles that emerged during its development stand to enable the more efficient and flexible preparation of a wide range of natural products, pharmaceuticals, and intermediates that possess a stereogenic allene motif. This new reaction was harnessed to achieve the first completely stereocontrolled total synthesis of (-)-peridinin. This synthesis was accomplished using only one reaction iteratively to assemble four fully functionalized building blocks with complete stereoretention at each initial halide or boron-bearing carbon. This synthesis elevates the capacity of the iterative cross-coupling strategy to an unprecedented benchmark. Moreover, the efficient and highly modular nature of this synthesis promises to enable systematic dissection of the heretofore enigmatic structure/function relationships that underlie the protein-like antilipoperoxidant activities of this remarkable small molecule natural product.
