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92002-48-7

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92002-48-7 Usage

General Description

20-BROMO-1-EICOSANOL is a organic compound that belongs to the family of icosanols, which are long-chain aliphatic alcohols derived from fatty acids. This specific compound contains a bromine atom attached to the 20th carbon of the carbon chain. It is primarily used in organic synthesis and research as a reagent or building block for creating other organic compounds. It is a white solid at room temperature with a melting point of approximately 85 degrees Celsius. 20-BROMO-1-EICOSANOL has limited commercial applications and is mainly used in laboratory settings for its role in chemical reactions and structural determination.

Check Digit Verification of cas no

The CAS Registry Mumber 92002-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,0 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 92002-48:
(7*9)+(6*2)+(5*0)+(4*0)+(3*2)+(2*4)+(1*8)=97
97 % 10 = 7
So 92002-48-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H41BrO/c21-19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18-20-22/h22H,1-20H2

92002-48-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 20-bromoicosan-1-ol

1.2 Other means of identification

Product number -
Other names 20-bromoicosane-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:92002-48-7 SDS

92002-48-7Relevant articles and documents

Electrochemistry of Cytochrome c at a Lipid Langmuir Blodgett Monolayer Electrode

Nakashima, Naotoshi,Abe, Kazuhiro,Hirohashi, Toshiaki,Hamada, Keiko,Kunitake, Masashi,Manabe, Osamu

, p. 1021 - 1024 (1993)

Cytochrome c was found to undergo electron transfer reactions at a gold electrode modified with a Langmuir-Blodgett monolayer of 20-mercaptoeicosane-1-ol/dioleoyl-L-α-phosphatidylcholine (molar ratio, 1/20).The stability of the monolayer and the adsorption behavior of cytochrome c to the monolayer was also examined.

Cysteine-Targeted Insecticides against A. gambiae Acetylcholinesterase Are Neither Selective nor Reversible Inhibitors

Gorecki, Lukas,Andrys, Rudolf,Schmidt, Monika,Kucera, Tomas,Psotka, Miroslav,Svobodova, Barbora,Hrabcova, Veronika,Hepnarova, Vendula,Bzonek, Petr,Jun, Daniel,Kuca, Kamil,Korabecny, Jan,Musilek, Kamil

, p. 65 - 71 (2019/12/25)

Acetylcholinesterase cysteine-targeted insecticides against malaria vector Anopheles gambia and other mosquitos have already been introduced. We have applied the olefin metathesis for the preparation of cysteine-targeted insecticides in high yields. The prepared compounds with either a succinimide or maleimide moiety were evaluated on Anopheles gambiae and human acetylcholinesterase with relatively high irreversible inhibition of both enzymes but poor selectivity. The concept of cysteine binding was not proved by several methods, and poor stability was observed of the chosen most potent/selective compounds in a water/buffer environment. Thus, our findings do not support the proposed concept of cysteine-targeted selective insecticides for the prepared series of succinimide or maleimide compounds.

Preparation of ω-functionalized eicosane-phosphate building blocks

Jablonkai, Istvan,Oroszlan, Peter

, p. 103 - 112 (2007/10/03)

New 1,20-substituted eicosanes carrying phosphate headgroups and readily derivatizable thiol, maleimido, and activated carboxylic ester moieties were prepared. The C20-backbone of these molecules was assembled by a halopolycarbon homologation from 1,8-dichlorooctane and 1,6-dibromohexane. 20-Mercapto- and 20-maleimido-icosylphosphates were synthesized via ω-bromo di-t-butyl protected icosylphosphate while 20-phosphonooxy- icosanoic acid N-hydroxysuccinimidoyl ester was prepared via ω-bromo dibenzyl protected icosylphosphate in multistep syntheses. These molecules can serve as model compounds for studying binding and structural organization on different surfaces with potential applications in the fields of biosensors.

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