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56784-04-4

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56784-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56784-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,7,8 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56784-04:
(7*5)+(6*6)+(5*7)+(4*8)+(3*4)+(2*0)+(1*4)=154
154 % 10 = 4
So 56784-04-4 is a valid CAS Registry Number.

56784-04-4SDS

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 methyl 2-trimethylsiloxytetracosanoate

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:56784-04-4 SDS

56784-04-4Downstream Products

56784-04-4Relevant articles and documents

Biologically Active Glycosides from Asteroidea, XIII. - Glycosphingolipids from the Starfish Acanthaster planci, 2.- Isolation and Structure of Six New Cerebrosides

Kawano, Yasuhiro,Higuchi, Ryuichi,Isobe, Ryuichi,Komori, Tetsuya

, p. 19 - 24 (2007/10/02)

Six new cerebrosides (ceramide monohexosides), acanthacerebroside A (1), B (2), C (3), D (4), E (5), and F (6) were isolated from the water-insoluble lipid fraction of the chloroform-methanol extract of the starfish Acanthaster planci.On the basis of chemical and spectral evidences, they were characterized as 1-O-(β-D-glucopyranosyl)-substituted (2S,3S,4R)-2--1,3,4-hexadecanetriol (1), (2S,3S,4R)-2--1,3,4-docosanetriol (2), (2S,3S,4R,13Z)-2--13-docosene-1,3,4-triol (3), (2S,3R,4E,10E)-2--4,10-octadecadiene-1,3-diol (4), (2S,3R,4E,10E)-2--4,10-octadecadiene-1,3-diol (5), and (2S,3R,4E,10E)-2--4,10-octadecadiene-1,3-diol (6).Reversed-phase HPLC was effective to isolate these cerebrosides revealing the very close resemblance in structure.Negative FABMS spectrometry was useful in providing information on the molecular mass of the cerebrosides.

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