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1069-72-3

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1069-72-3 Usage

Description

2-BROMO-N,N-DIETHYLETHYLAMINE HYDROBROMIDE, with the molecular formula C6H15Br2N, is a white to off-white crystalline solid that exhibits solubility in both water and organic solvents. This chemical compound serves as a crucial pharmaceutical intermediate in the synthesis of a variety of drugs and is also employed as a reagent in organic chemistry for the preparation of other compounds. Its potential applications in the medical and pharmaceutical industries are currently being explored through research and development activities. However, due to its potential health hazards, it is essential to handle this chemical with care.

Uses

Used in Pharmaceutical Industry:
2-BROMO-N,N-DIETHYLETHYLAMINE HYDROBROMIDE is used as a pharmaceutical intermediate for the synthesis of various drugs, contributing to the development of new medications and therapeutic agents.
Used in Organic Chemistry:
In the realm of organic chemistry, 2-BROMO-N,N-DIETHYLETHYLAMINE HYDROBROMIDE is utilized as a reagent for the preparation of other compounds, facilitating chemical reactions and the creation of new substances.
Used in Research and Development:
2-BROMO-N,N-DIETHYLETHYLAMINE HYDROBROMIDE is employed in research and development activities to explore its potential applications in the medical and pharmaceutical industries, aiming to discover new uses and enhance existing ones.

Check Digit Verification of cas no

The CAS Registry Mumber 1069-72-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1069-72:
(6*1)+(5*0)+(4*6)+(3*9)+(2*7)+(1*2)=73
73 % 10 = 3
So 1069-72-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H14BrN/c1-3-8(4-2)6-5-7/h3-6H2,1-2H3

1069-72-3 Well-known Company Product Price

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  • Aldrich

  • (453064)  2-Bromo-N,N-diethylethylaminehydrobromide  98%

  • 1069-72-3

  • 453064-25G

  • 1,788.93CNY

  • Detail
  • Aldrich

  • (453064)  2-Bromo-N,N-diethylethylaminehydrobromide  98%

  • 1069-72-3

  • 453064-100G

  • 5,335.20CNY

  • Detail

1069-72-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-N,N-diethylethylamine hydrobromide

1.2 Other means of identification

Product number -
Other names 2-Bromoethyldiethylamine Hydrobromide

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:1069-72-3 SDS

1069-72-3Upstream product

1069-72-3Relevant articles and documents

Transition Metal Complexes with Sulfur Ligands, 138 Synthesis, Structures, and Reactions of Sulfur-Rich Nickel and Platinum Complexes with [MS3] and [MNS2] Cores

Sellmann, Dieter,Haeussinger, Daniel,Heinemann, Frank W.

, p. 1715 - 1726 (2007/10/03)

Nickel and platinum complexes with tridentate ligands, having [S3] or [NS2] donor sets were investigated in order to model active sites of enzymes such as hydrogenases or CO dehydrogenases. Starting from diphenyl sulfide, a preparative synthesis was developed for 'S3'-H2 ['S3'-H2=bis(2-mercaptophenyl) sulfide]. Reactions of 'S3'-H2 or anionic 'S3'(2-) with nickel and platinum precursors resulted in the formation of binuclear [Ni('S3')]2 (1) and trinuclear [Pt('S3')]3 (5). Complex 1 was cleaved by PMe3 or CN(1-) to give the mononuclear complexes [Ni('S3')(PMe3)] (2) and NMe4[Ni('S3')(CN)] (3). Attempts to coordinate hydride to the [Ni('S3')] fragment led to C-S bond cleavage of the ligand and formation of (NMe4)2[{Ni(μ-SC6H5)(S2C6H4)}2] (4). Oxidative addition of Li['S3'-H] to [Pt(PPh3)4] afforded the platinum hydride complexes Li[Pt(H)('S3')] and Li[Pt(H)(PPh3)('S3')] which, however, could not be separated from each other and yielded [Pt('S3')(PPh3)] (6) when treated with MeOH. In order to investigate electronic effects of the donor set, the 'S3' ligand was modified by alkylation of one thiol group to give 'RS3'-H derivatives (R=Me, Et, Cy) and by replacing a mercaptophenyl unit by an amine in 'Et2NS2'-H ['Et2NS2'-H=N,N-diethyl-2-(2-mercaptothiophenyl)ethylamine]. Reactions of Ni(II) or Ni(0) compounds with these ligands in a 1:1 ratio yielded the 1:2 complexes [Ni('MeS3')2] (7), [Ni('EtS3')2] (9) and [Ni('CyS3')2] (10), with 'RS3'(1-) acting as bidentate ligands only. Complex 7 reversibly reacted with PMe3 to form cis-[Ni(PMe3)2('MeS3')2] (8), exhibiting monodentate 'MeS3' ligands. [Ni('Et2HNS2')2]Br2 (11) reeacted reversibly with bases to presumably give octahedral [Ni('Et2NS2')2]. Complexes 7, 9 and 10 also did not yield any [Ni('RS3')(H)] hydride complex when treated with hydride sources. Oxidative addition of 'CyS3'-H to [Pt(PPh3)4] yielded the hydride complexes [Pt(H)('CyS3')] and [Pt(H)(PPh3)('CyS3')] which, however, formed an inseparable mixture and underwent C-S bond cleavage when heated, affording [Pt(o-S2C6H4)(PPh3)2]. The molecular structures of 1, 2, 3, 5, 6, 7, and 11 were determined by X-ray crystallography, revealing butterfly-like shapes for the [MS3L] cores of the complexes.

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