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1,7,13-Trioxa-4,10,16-triazacyclooctadecane-4-ethanol, 10,16-bis(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

587874-99-5

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587874-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 587874-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,7,8,7 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 587874-99:
(8*5)+(7*8)+(6*7)+(5*8)+(4*7)+(3*4)+(2*9)+(1*9)=245
245 % 10 = 5
So 587874-99-5 is a valid CAS Registry Number.

587874-99-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(10,16-Dibenzyl-1,7,13-trioxa-4,10,16-triaza-cyclooctadec-4-yl)-ethanol

1.2 Other means of identification

Product number -
Other names -

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:587874-99-5 SDS

587874-99-5Relevant academic research and scientific papers

MRI sensing of neurotransmitters with a crown ether appended Gd3+ complex

Oukhatar, Fatima,Même, Sandra,Même, William,Szeremeta, Frédéric,Logothetis, Nikos K.,Angelovski, Goran,Tóth, éva

, p. 219 - 225 (2015/03/04)

Molecular magnetic resonance imaging (MRI) approaches that detect biomarkers associated with neural activity would allow more direct observation of brain function than current functional MRI based on blood-oxygen-level-dependent contrast. Our objective wa

A substituted triaza crown ether as a binding site in DNA conjugates

Vogel, Stefan,Rohr, Katja,Dahl, Otto,Wengel, Jesper

, p. 1006 - 1007 (2007/10/03)

Synthesis of an asymmetrically substituted triaza crown ether, its incorporation into the 3′-end and 5′-end of nine-mer oligonucleotides, and the influence of various alkanediamine ligands on duplex thermostabilities are reported.

Synthesis of an asymmetrically substituted AZA crown ether as metal and amino acid binding site in DNA conjugates

Vogel, Stefan,Rohr, Katja,Dahl, Otto,Wengel, Jesper

, p. 1039 - 1040 (2007/10/03)

Crown ether 4 as a receptor core for protonated primary amines such as amino acids has been synthesized and incorporated into oligodeoxynucleotides as dangling ends.

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