51575-83-8 Usage
Description
1-Chloro-2-octyne is a propargyl halide, which is an organic compound characterized by the presence of a triple bond (alkyne) and a chlorine atom. It is known for its reactivity in various chemical reactions, particularly in the formation of 1,5-diynes through reactions with other compounds.
Uses
1. Used in Chemical Synthesis:
1-Chloro-2-octyne is used as a key intermediate in the synthesis of 1,5-diynes. It is particularly useful for this application due to its reactivity and the ability to form meta-depside bonds with other compounds.
2. Used in Organic Chemistry:
In the field of organic chemistry, 1-chloro-2-octyne is used as a building block for the creation of more complex organic molecules. Its unique structure allows for a variety of reactions, making it a versatile compound for researchers and chemists.
3. Used in Pharmaceutical Research:
1-Chloro-2-octyne may also find applications in the development of new pharmaceutical compounds. Its reactivity and ability to form various bond types can be exploited to create novel drug candidates with potential therapeutic properties.
4. Used in Material Science:
The unique properties of 1-chloro-2-octyne can be utilized in the development of new materials with specific characteristics. Its ability to form stable bonds with other compounds can contribute to the creation of materials with tailored properties for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 51575-83-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,7 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51575-83:
(7*5)+(6*1)+(5*5)+(4*7)+(3*5)+(2*8)+(1*3)=128
128 % 10 = 8
So 51575-83-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H13Cl/c1-2-3-4-5-6-7-8-9/h2-5,8H2,1H3
51575-83-8Relevant articles and documents
Aromatic cation activation of alcohols: Conversion to alkyl chlorides using dichlorodiphenylcyclopropene
Kelly, Brendan D.,Lambert, Tristan H.
supporting information; experimental part, p. 13930 - 13931 (2009/12/25)
(Chemical Equation Presented) A novel paradigm for the activation of alcohols toward nucleophilic displacement via formation of cyclopropenium ethers is described. The conversion of a range of alcohol substrates to the corresponding alkyl chlorides occurs rapidly upon treatment with 3,3-dichloro-1,2-diphenylcyclopropene. 1H NMR data support the intermediacy of a cyclopropenium intermediate, and the reaction is demonstrated to proceed primarily via the SN2 mechanism for 1-phenylethanol. A total of 12 examples of substrate scope are provided.
