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57666-61-2

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57666-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57666-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,6 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57666-61:
(7*5)+(6*7)+(5*6)+(4*6)+(3*6)+(2*6)+(1*1)=162
162 % 10 = 2
So 57666-61-2 is a valid CAS Registry Number.

57666-61-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-hexoxyphenyl)azanium,chloride

1.2 Other means of identification

Product number -
Other names p-Aminophenyl-n-hexyl ether hydrochloride

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:57666-61-2 SDS

57666-61-2Relevant articles and documents

High-Density Noncovalent Functionalization of DNA by Electrostatic Interactions

Chen, Wei,Gerasimov, Jennifer Y.,Zhao, Pei,Liu, Kai,Herrmann, Andreas

, p. 12884 - 12889 (2015)

Preserving DNA hybridization in organic solvents could someday serve to significantly extend the applicability of DNA-based technologies. Here, we present a method that can be used to solubilize double-stranded DNA at high concentrations in organic media.

Effect of Molecular Structure on Mesomorphism. 22. Liquid Crystalline 1-Alkanol Derivatives

Griffin, A. C.,Vaidya, S. R.

, p. 85 - 88 (2007/10/02)

Several 1-alkanols having a mesogenic unit attached to the omega-carbon have been prepared.Many of these are liquid crystalline.The nematic mesophase is predominant for these materials.This is presumably due to intermolecular hydrogen-bonding between polar terminal groups such as cyano or nitro and the primary hydroxyl functionality of a proximal molecule.The resulting end-to-end association favors a nematic mesophase.

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