1,1′-Diethyl-2,2′-dicarbocyanine iodide
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1,1′-Diethyl-2,2′-dicarbocyanine iodide
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CAS No:
14187-31-6
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Formula:
C27H27N2.I
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Chemical Name:
1,1′-Diethyl-2,2′-dicarbocyanine iodide
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Synonyms:
Quinolinium,1-ethyl-2-[5-(1-ethyl-2(1H)-quinolinylidene)-1,3-pentadien-1-yl]-,iodide (1:1);Quinolinium,1-ethyl-2-[5-(1-ethyl-2(1H)-quinolylidene)-1,3-pentadienyl]-,iodide;Quinolinium,1-ethyl-2-[5-(1-ethyl-2(1H)-quinolinylidene)-1,3-pentadienyl]-,iodide;1-Ethyl-2-[5-(1-ethyl-2(1H)-quinolylidene)-1,3-pentadienyl]quinolinium iodide;1,1′-Diethyl-2,2′-dicarbocyanine iodide;1,1′-Diethyl-2,2′-quinodicarbocyanine iodide;2,2′-Dicarbocyanine iodide,1,1′-diethyl-;1,1′-Diethyldicarbocyanine iodide;NK 1456;Diethyldicarbocyanine iodide;Eastman 9618;DDCI dye;DDI;DDI (dye)
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CAS No:
Safety Information
UN 2811 6.1/PG 2
R20/21/22; R36/37/38
S24/25; S36; S26
Xn
P261; P280; P305 + P351 + P338
H302; H312; H315; H319; H332; H335
|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
1,1′-Diethyl-2,2′-dicarbocyanine iodide Use and Manufacturing
2, 3-Dibromopentane, an organic synthetic intermediate that occupies an important position in the field of organic chemistry, its unique chemical properties and wide applicability make it play an indispensable role in scientific research and industrial production. This compound contains two bromine atoms in its molecular structure, which gives it a high degree of reactivity and diversity, enabling it to participate in and catalyze a range of complex organic chemical reactions. In organic synthesis, the application of 2, 3-Dibromopentane is quite versatile. It can react with organic compounds of magnesium metal through the classical Grignard reaction to form a series of alkyl or aryl compounds, which have important applications in medicine, plastics, dyes and many other fields. In addition, 2, 3-Dibromopentane can also be converted into a variety of structurally complex organic molecules through substitution reactions, such as SN1 or SN2 reactions, providing chemists with a wealth of synthetic tools. Further, 2, 3-Dibromopentane shows strong potential for the preparation of biologically active heterocyclic compounds. For example, it can be used as a precursor to generate five - or six-membered heterocyclic structures containing bromine through cyclization, which are of great value in drug development. Studies have shown that brominated heterocyclic compounds show excellent biological activities in the fields of anticancer, antibacterial, antiviral, etc. Therefore, 2, 3-Dibromopentane has broad application prospects in pharmaceutical innovation. In the pharmaceutical industry, the application of 2, 3-dibromopentane is more direct and critical. It can be used as a raw material to synthesize some chiral drug intermediates, chiral drugs often show higher selectivity and efficacy in the treatment of diseases, so it has an important position in drug design and development. At the same time, 2, 3-Dibromopentane has also found its application in the field of pesticides. Through the chemical reaction it participates in, it can synthesize the active ingredients of bromine pesticides with high efficiency and low toxicity, which has played a role in promoting the sustainable development of modern agriculture. With its unique chemical properties and wide applicability, 2, 3-Dibromopentane provides rich synthetic strategies and innovation possibilities for many fields such as organic chemistry, medicine and pesticides. With the continuous progress of chemical science and the in-depth exploration of new organic compounds, the application potential of 2, 3-Dibromopentane will be further explored, and it will play a greater role in the future scientific research and industrial production.
Quinolinium, 1-ethyl-2-[5-(1-ethyl-2(1H)-quinolinylidene)-1,3-pentadien-1-yl]-, iodide (1:1): INACTIVE
Computed Properties
Molecular Weight:506.4
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:506.12190
Monoisotopic Mass:506.12190
Topological Polar Surface Area:7.1
Heavy Atom Count:30
Complexity:591
Undefined Bond Stereocenter Count:3
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
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