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4-IODO-2,5-DIMETHOXYPHENETHYLAMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69587-11-7

69587-11-7 Suppliers

This product is a nationally controlled contraband or patented product, and the Lookchem platform doesn't provide relevant sales information.

69587-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69587-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,8 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69587-11:
(7*6)+(6*9)+(5*5)+(4*8)+(3*7)+(2*1)+(1*1)=177
177 % 10 = 7
So 69587-11-7 is a valid CAS Registry Number.

69587-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-iodo-3-methoxyphenyl)-2-methoxyethanamine

1.2 Other means of identification

Product number -
Other names 1-(2,5-dimethoxy-4-iodophenyl)-2-aminoethane

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:69587-11-7 SDS

69587-11-7Relevant academic research and scientific papers

Synthesis of 25X-BOMes and 25X-NBOHs (X = H, I, Br) for pharmacological studies and as reference standards for forensic purposes

Alves de Barros, Wellington,Queiroz, Marcelo Pereira,da Silva Neto, Leonardo,Borges, Graziele Martins,Martins, Felipe Terra,de Fátima, ?ngelo

supporting information, (2021/01/28)

An expeditious method is reported for the synthesis of three NBOHs (25H-, 25I- and 25B-NBOH; 9–38% overall yield) and three NBOMes (25H-, 25I- and 25B-NBOMe; 7–33% overall yield) from salicylaldehyde and 2-methoxyaldehyde, respectively. The X-ray structures of 25H-, 25I- and 25B-NBOH.HCl were also determined. Our approach should provide a general entry for preparing such a class of substances for pharmacological and forensic purposes.

Nanosensor for Sensitive Detection of the New Psychedelic Drug 25I-NBOMe

Alfonso, María,Díaz de Gre?u, Borja,Garrido, Eva,Gavi?a, Pablo,Lozano-Torres, Beatriz,Marcos, M. Dolores,Martínez-Má?ez, Ramón,Parra, Margarita,Sancenón, Félix

, (2020/02/27)

This work reports the synthesis, characterization, and sensing behavior of a hybrid nanodevice for the detection of the potent abuse drug 25I-NBOMe. The system is based on mesoporous silica nanoparticles, loaded with a fluorescent dye, functionalized with

Synthesis and identification of metabolite biomarkers of 25C-NBOMe and 25I-NBOMe

Wu, Xiongyu,Eriksson, Caroline,Wohlfarth, Ariane,Wallgren, Jakob,Kronstrand, Robert,Josefsson, Martin,Dahlén, Johan,Konradsson, Peter

, p. 6393 - 6400 (2017/10/16)

Synthetic routes have been developed for synthesis of potential metabolites of 25C-NBOMe and 25I-NBOMe. Nine potential metabolites have been synthesized, among which compounds 8 and 20a could be used as metabolite biomarkers of 25C-NBOMe and 20b of 25I-NB

4-Aryl-substituted 2,5-dimethoxyphenethylamines: Synthesis and serotonin 5-HT2A receptor affinities

Trachsel, Daniel,Nichols, David E.,Kidd, Stephanie,Hadorn, Marcel,Baumberger, Franz

experimental part, p. 692 - 704 (2010/04/23)

A series of novel ligands for the serotonin 5-HT2A/C receptor subtype bearing the 2-phenylethylamine pharmacophore was synthesized and assayed for its 5-HT2A receptor binding affinity. As the 4′-arylsubstituted 2-(2,5-dimethoxyphenyl

Synthesis of deuterium labeled phenethylamine derivatives

Xu, Ya-Zhu,Chen, Chinpiao

, p. 1187 - 1200 (2008/04/18)

The synthesis of a series of five deuterium labeled phenethylamine derivatives, 4-bromo-2,5-[2H6]-dimethoxyphenethylamine (2C-B), 4-chloro-2,5-[2H6]-dimethoxyphenethylamine (2C-C), 2,5-[2H6]-dimethoxy-4-iodophenethylamine (2C-I), 2,5-[2H6]-dimethoxy-4-ethylthiophenethylamine (2C-T-2) and 2,5-[2H6]-dimethoxy-4-n-propylthiophenethylamine (2C-T-7) from 1,4-[2H6]-dimethoxybenzene is described. The isotopically labeled compounds are used as internal standards in gas chromatography-mass spectrometry (GC-MS) assays. Copyright