56318-83-3 Usage
Description
(2E)-1-bromooct-2-ene, with the molecular formula C8H15Br, is a colorless liquid and a chemical compound belonging to the class of alkenes. It has a molecular weight of 193.11 g/mol and features a double bond between the second and third carbon atoms. The bromine atom attached to the molecule classifies it as a bromoalkene, which contributes to its reactivity and specificity in chemical reactions. This unique structure and versatility make (2E)-1-bromooct-2-ene valuable in various industrial applications.
Uses
Used in Organic Synthesis:
(2E)-1-bromooct-2-ene is used as a key intermediate in organic synthesis for the production of a variety of chemicals and materials. Its reactivity and specific chemical properties allow for the creation of new compounds through various chemical reactions.
Used in Chemical Production:
(2E)-1-bromooct-2-ene serves as a building block in the production of other chemicals and materials. Its unique structure and versatility make it an essential component in the synthesis of a wide range of industrial products.
Used in Pharmaceutical Industry:
(2E)-1-bromooct-2-ene is used as a starting material or intermediate in the synthesis of pharmaceutical compounds. Its reactivity and specific chemical properties enable the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
(2E)-1-bromooct-2-ene is utilized in the development of agrochemicals, such as pesticides and herbicides. Its unique chemical structure allows for the creation of effective and targeted agricultural products.
Used in Material Science:
(2E)-1-bromooct-2-ene is employed in the field of material science for the development of new materials with specific properties. Its versatility and reactivity contribute to the creation of innovative materials for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 56318-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,1 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56318-83:
(7*5)+(6*6)+(5*3)+(4*1)+(3*8)+(2*8)+(1*3)=133
133 % 10 = 3
So 56318-83-3 is a valid CAS Registry Number.
56318-83-3Relevant articles and documents
Enantioselective synthesis of 3-substituted dihydrobenzofurans through iridium-catalyzed intramolecular hydroarylation
Nishimura, Takahiro,Sakamoto, Kana
supporting information, p. 684 - 690 (2021/02/06)
Intramolecular hydroarylationviaC-H activation is one of the most powerful methods to synthesize carbo- and heterocyclic compounds, whereas we still have room for developing a highly enantioselective variant of the reaction. Here we describe Ir-catalyzed enantioselective intramolecular hydroarylation ofm-allyloxyphenyl ketones. The enantioselective cyclization was efficiently catalyzed by a cationic iridium complex coordinated with a conventional chiral bisphosphine ligand to give benzofurans in high yields with high enantioselectivity. A carbonyl group of ketones functioned as an effective directing group for the C-H activation. In terms of synthetic utility, we also achieved one-pot synthesis of chiral 3-substituted dihydrobenzofurans from readily available allylic carbonates andm-hydroxyacetophenonesviasequential Pd-catalyzed allylic substitution and Ir-catalyzed intramolecular hydroarylation.
Synthesis method of 3-azidopropylsilane
-
Paragraph 0039; 0040, (2020/06/05)
The invention discloses a synthetic method of 3-azidopropylsilane, wherein the method comprises the steps: firstly, allyl azide is synthesized by allyl bromide, and because the allyl azide is easy togenerate [3,3] rearrangement reaction at room temperatur
BOTPPI, a new Wittig salt for the synthesis of 12-(S)-hydroxy- eicosatetraenoic acid [12-(S)-HETE]
Christiansen, Michael A.,Andrus, Merritt B.
, p. 4805 - 4808 (2012/09/22)
An efficient route to (Z)-(8-benzyloxy-8-oxooct-3-en-1-yl) triphenylphosphonium iodide, or BOTPPI, is disclosed, complete with full experimental details, NMR spectra, and HRMS data. BOTPPI serves as a surrogate for (Z)-(8-methoxy-8-oxooct-3-en-1-yl)triphe
