37051-38-0 Usage
Uses
Used in Pharmaceutical Industry:
(4-Iodophenyl)acetyl chloride is used as a reagent for the synthesis of pharmaceutical intermediates. Its reactivity allows for the creation of a wide range of organic compounds that can be further utilized in the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, (4-Iodophenyl)acetyl chloride is employed as a precursor in the synthesis of various agrochemicals. Its ability to participate in multiple chemical reactions makes it a valuable component in the development of pesticides and other agricultural products.
Used in Dye Industry:
(4-Iodophenyl)acetyl chloride is used as a starting material for the synthesis of dyes. Its versatility in organic synthesis contributes to the production of a diverse array of dyes used in various applications, including textiles and printing inks.
Used in Organic Synthesis:
(4-Iodophenyl)acetyl chloride is used as a versatile building block in organic synthesis. Its reactivity with the acetyl chloride functional group enables it to undergo a variety of chemical reactions, making it an essential tool for the synthesis of complex organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 37051-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,5 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 37051-38:
(7*3)+(6*7)+(5*0)+(4*5)+(3*1)+(2*3)+(1*8)=100
100 % 10 = 0
So 37051-38-0 is a valid CAS Registry Number.
37051-38-0Relevant academic research and scientific papers
Vaulted biaryls in catalysis: A structure-activity relationship guided tour of the immanent domain of the VANOL ligand
Guan, Yong,Ding, Zhensheng,Wulff, William D.
, p. 15565 - 15571 (2013/11/19)
The active site in the BOROX catalyst is a chiral polyborate anion (boroxinate) that is assembled in situ from three equivalents of B(OPh) 3 and one of the VANOL ligand by a molecule of substrate. The substrates are bound to the boroxinate by Hbonds to oxygen atoms O1-O3. The effects of introducing substituents at each position of the naphthalene core of the VANOL ligand are systematically investigated in an aziridination reaction. Substituents in the 4,4′- and 8,8′-positions have a negative effect on catalyst performance, whereas, substituents in the 7- and 7′-positions have the biggest impact in a positive direction. VANOL destination: The active site in the BOROX catalyst is a chiral polyborate anion (boroxinate; see figure) that is assembled in situ from three equivalents of B(OPh)3 and one of the VANOL ligand by a molecule of substrate. The effects of introducing substituents at each position of the naphthalene core of the VANOL ligand are systematically investigated in an aziridination reaction. Copyright
