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5-methyl-1-[3-({[36,37,38,39,40,41,42,43,44,45,46,47,48,49-tetradecahydroxy-10,15,20,25,30,35-hexakis(hydroxymethyl)-2,4,7,9,12,14,17,19,22,24,27,29,32,34-tetradecaoxaoctacyclo[31.2.2.2~3,6~.2~8,11~.2~13,16~.2~18,21~.2~23,26~.2~28,31~]nonatetracont-5-yl]m is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81644-56-6

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81644-56-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81644-56-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,4 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81644-56:
(7*8)+(6*1)+(5*6)+(4*4)+(3*4)+(2*5)+(1*6)=136
136 % 10 = 6
So 81644-56-6 is a valid CAS Registry Number.

81644-56-6SDS

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 6-deoxy-6-<(3-thym-1-yl)propyl)thio>-β-cyclodextrin

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:81644-56-6 SDS

81644-56-6Downstream Products

81644-56-6Relevant academic research and scientific papers

Nucleobase-Functionalized β-Cyclodextrins. Preparation and Spectral Properties

Nagai, Katsuyuki,Hayakawa, Kenji,Kanematsu, Ken

, p. 1022 - 1027 (1984)

The nucleobase-functionalized β-cyclodextrins in which a nucleobase was linked to C-6 of β-cyclodextrin directly or through a flexible carbon chain were synthesized.Their structures were determined on the basis of spectroscopic data and elemental analyses.Fast atom bombardment mass spectrometry was employed to determine the molecular weight of these nonvolatile compounds.The specific interaction of the nucleobase moiety with the cyclodextrin cavity, the influence of chain length on their inclusion abilities, and the pH-dependent conformational change of these compounds are dicussed on the basis of analyses of these molecules by UV and circular dichroism spectra.

SYNTHESIS OF NUCLEIC ACID BASE FUNCTIONALIZED β-CYCLODEXTRINS: THE NUCLEOSIDE ANALOGUE

Nagai, Katsuyuki,Kondo, Hirosato,Tsuruzoe, Nobutomo,Hayakawa, Kenji,Kanematsu, Ken

, p. 53 - 56 (2007/10/02)

The β-cyclodextrins functionalized with the nitrogen-bases of nucleic acid such as thymine, uracil, cytosine, and adenine by a flexible polymethylene bridge have been synthesized and their structures were determined on the basis of the spectroscopic data.

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