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516462-74-1

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516462-74-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 516462-74-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,6,4,6 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 516462-74:
(8*5)+(7*1)+(6*6)+(5*4)+(4*6)+(3*2)+(2*7)+(1*4)=151
151 % 10 = 1
So 516462-74-1 is a valid CAS Registry Number.

516462-74-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-[bis(4-methoxyphenyl)-phenylmethoxy]ethylamino]ethanol

1.2 Other means of identification

Product number -
Other names Ethanol,2-[[2-[bis(4-methoxyphenyl)phenylmethoxy]ethyl]amino]

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:516462-74-1 SDS

516462-74-1Relevant articles and documents

Modified oligonucleotides and compound that can be used for synthesizing same

-

Paragraph 0129-0130; 0131-0132, (2020/12/08)

The present disclosure falls within the field of biomedical technology, and in particular relates to modified oligonucleatides and a compound that can be used for synthesizing same and a method for modifying oligonucleotides. The present disclosure also relates to the use of the modified oligonucleotides for preventing and/or treating diseases associated with the liver in a subject.

Synthesis of triple helix forming oligonucleotides with a phenanthroline moiety into the 3′-3′ inversion site of polarity

Esposito, Veronica,Galeone, Aldo,Mayol, Luciano,Oliviero, Giorgia,Randazzo, Antonio,Varra, Michela

, p. 4228 - 4233 (2007/10/03)

A protocol for the synthesis of triplex forming oligonucleotides containing a chelating molecule in the 3′-3′ inversion site of polarity is reported. A number of 16-mers have been synthesized and UV spectroscopy employed to evaluate the stability of their triple helix complexes with the pertinent double-strand oligonucleotide targets. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2002.

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