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20188-65-2

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20188-65-2 Usage

General Description

1-C-1H-benzimidazol-2-ylhexitol is a chemical compound with a complex structure that consists of a benzimidazole ring attached to a hexitol moiety. It is often used in organic synthesis and pharmaceutical research due to its potential as a building block for various organic compounds. The compound's unique structure makes it a valuable tool in the development of new drugs and materials. Additionally, its benzimidazole ring has been found to exhibit biological activity, making it a potentially important pharmacophore in drug design. Further research and exploration of 1-C-1H-benzimidazol-2-ylhexitol's properties and applications may lead to its use in medical treatments and other industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 20188-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,8 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20188-65:
(7*2)+(6*0)+(5*1)+(4*8)+(3*8)+(2*6)+(1*5)=92
92 % 10 = 2
So 20188-65-2 is a valid CAS Registry Number.

20188-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1H-benzimidazol-2-yl)hexane-1,2,3,4,5,6-hexol

1.2 Other means of identification

Product number -
Other names 2-<D-glycero-D-gulo-1,2,3,4,5,6-Hexahydroxy-hexyl>-benzimidazol

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:20188-65-2 SDS

20188-65-2Downstream Products

20188-65-2Relevant articles and documents

Theoretical study of the experimental coordination behavior of N-(2-aminophenyl)-d-glycero-d-gulo-heptonamide to Hg(II) ion

Bernal-Uruchurtu, Margarita I.,Metta-Magana, Alejandro J.,Guerrero-Alvarez, Jorge A.,Reyes-Martinez, Reyna,Tlahuext, Hugo

, p. 2804 - 2812 (2008)

The reactivity of N-(2-aminophenyl)-d-glycero-d-gulo-heptonamide (adgha), with the group 12 cations, Zn(II), Cd(II), and Hg(II), was studied in DMSO-d6 solution. The studied system showed a selective coordination to Hg(II), and the products formed were characterized by 1H and 13C NMR in DMSO-d6 solution and fast atom bombardment (FAB+) mass spectra. The expected coordination compounds, [Hg(adgha)](NO3)2 and [Hg(adgha)2](NO3)2, were observed as unstable intermediates that decompose to bis-[2-(d-glycero-d-gulo-hexahydroxyhexyl)-benzimidazole-κN]mercury(II) dinitrate, [Hg(ghbz)2](NO3)2. The chemical transformation of the complexes was followed by NMR experiments, and the nature of the species formed is sustained by a theoretical study done using DFT methodology. From this study, we propose the structure of the complexes formed in solution, the relative stability of the species formed, and the possible role of the solvent in the observed transformations.

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