57152-87-1 Usage
Uses
Used in Organic Synthesis:
1-chloro-10-iododecane is used as a reagent in organic synthesis for the preparation of alkyl iodides. Its unique structure allows for versatile reactions and the formation of a wide range of organic compounds.
Used in Organic Electronics:
1-chloro-10-iododecane has been investigated for its potential applications in the field of organic electronics. Its properties may contribute to the development of new electronic materials and devices.
Used as a Precursor for Synthesis:
Due to its structural features, 1-chloro-10-iododecane serves as a precursor for the synthesis of various organic compounds, enabling the creation of new molecules with specific functions and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 57152-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,5 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57152-87:
(7*5)+(6*7)+(5*1)+(4*5)+(3*2)+(2*8)+(1*7)=131
131 % 10 = 1
So 57152-87-1 is a valid CAS Registry Number.
57152-87-1Relevant academic research and scientific papers
Photon can tremendously accelerate the alkyl iodides' elimination in water
Liu, Wenbo,Li, Chao-Jun
supporting information, p. 1699 - 1702 (2015/03/14)
Elimination of the alkyl halides in water is very difficult due to the heterogeneous nature and the limitation of base strength. We discovered that ultra-violet (UV) light can enhance the elimination rate of alkyl iodides, including primary, secondary, and tertiary iodides in water dramatically for the first time. We propose a tandem radical-carbocation reaction mechanism to rationalize this special property of alkyl iodides.
Deiodinative fluorination of alkyl iodide with p-iodotoluene difluoride
Sawaguchi, Masanori,Hara, Shoji,Nakamura, Yutaka,Ayuba, Shinichi,Fukuhara, Tsuyoshi,Yoneda, Norihiko
, p. 3315 - 3319 (2007/10/03)
Oxidative fluorination of alkyl iodides with p-iodotoluene difluoride (4) was carried out. In the presence of Et3N-4HF, the fluorination reaction of prim-alkyl iodides selectively took place at the iodine position under mild conditions to give the corresponding alkyl fluorides in good yields.
