131894-91-2 Usage
Description
1-N-Heptyl-4-iodobenzene, with the molecular formula C16H25I, is an organic compound that features a benzene ring with a heptyl group (a seven-carbon chain) attached to the first carbon atom and an iodine atom attached to the fourth carbon atom of the benzene ring. 1-N-HEPTYL-4-IODOBENZENE is known for its versatility in chemical reactions and transformations due to the presence of the iodine atom, making it an important compound in various fields of chemistry.
Uses
Used in Organic Synthesis:
1-N-Heptyl-4-iodobenzene is used as a key intermediate in the synthesis of various organic compounds, contributing to the formation of complex molecules and structures.
Used in Pharmaceutical Production:
1-N-Heptyl-4-iodobenzene is utilized as a building block in the production of pharmaceuticals, playing a crucial role in the development of new drugs and medications.
Used in Agrochemical Production:
1-N-HEPTYL-4-IODOBENZENE is also used in the creation of agrochemicals, which are essential for enhancing crop protection and agricultural productivity.
Used in Fine Chemicals Production:
1-N-Heptyl-4-iodobenzene is employed in the synthesis of fine chemicals, which are high-purity chemicals used in various industries, including cosmetics, fragrances, and specialty chemicals.
Used as a Research and Laboratory Reagent:
In research and laboratory settings, 1-N-Heptyl-4-iodobenzene serves as a reagent for conducting experiments and exploring new chemical reactions and processes. Its unique structure and properties make it a valuable tool for scientific investigation.
Check Digit Verification of cas no
The CAS Registry Mumber 131894-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,8,9 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 131894-91:
(8*1)+(7*3)+(6*1)+(5*8)+(4*9)+(3*4)+(2*9)+(1*1)=142
142 % 10 = 2
So 131894-91-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H19I/c1-2-3-4-5-6-7-12-8-10-13(14)11-9-12/h8-11H,2-7H2,1H3
131894-91-2Relevant articles and documents
REACTIVE PERPENDICULAR ALIGNED MATERIAL, LIQUID CRYSTAL DISPLAY PANEL, AND METHOD OF LIQUID CRYSTAL ALIGNMENT
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Paragraph 0060, (2018/02/28)
The disclosure provides a reactive perpendicular aligned material, a liquid crystal display panel, and a method for aligning liquid crystals, a general structural formula of the reactive perpendicular aligned material is A-Z—R, A is —CH═CH—COOH; Z is wher
Design and synthesis of boronic acid inhibitors of endothelial lipase
O'Connell, Daniel P.,Leblanc, Daniel F.,Cromley, Debra,Billheimer, Jeffrey,Rader, Daniel J.,Bachovchin, William W.
scheme or table, p. 1397 - 1401 (2012/03/26)
Endothelial lipase (EL) and lipoprotein lipase (LPL) are homologous lipases that act on plasma lipoproteins. EL is predominantly a phospholipase and appears to be a key regulator of plasma HDL-C. LPL is mainly a triglyceride lipase regulating (V)LDL levels. The existing biological data indicate that inhibitors selective for EL over LPL should have anti-atherogenic activity, mainly through increasing plasma HDL-C levels. We report here the synthesis of alkyl, aryl, or acyl-substituted phenylboronic acids that inhibit EL. Many of the inhibitors evaluated proved to be nearly equally potent against both EL and LPL, but several exhibited moderate to good selectivity for EL.
