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503603-69-8

503603-69-8

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503603-69-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 503603-69-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,6,0 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 503603-69:
(8*5)+(7*0)+(6*3)+(5*6)+(4*0)+(3*3)+(2*6)+(1*9)=118
118 % 10 = 8
So 503603-69-8 is a valid CAS Registry Number.

503603-69-8SDS

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 (2R,2'R,5R,5'R)-5-((R,E)-1-(methoxymethoxy)oct-2-en-7-yn-1-yl)-5'-((R)-1-(methoxymethoxy)undecyl)octahydro-2,2'-bifuran

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:503603-69-8 SDS

503603-69-8Downstream Products

503603-69-8Relevant articles and documents

Process for preparing pentacene derivatives

-

, (2008/06/13)

A process for preparing substituted pentacene compounds comprises the step of cyclizing substituted bis(benzyl)phthalic acids using an acid composition comprising trifluoromethanesulfonic acid, the substituted bis(benzyl)phthalic acids being represented by the following general formulas: wherein each R (that is, each of the groups R1 through R8) is independently an electron-donating group, a halogen atom, a hydrogen atom, or a combination thereof.

Process for preparing pentacene derivatives

-

, (2008/06/13)

A process for preparing substituted pentacene compounds comprises the step of cyclizing substituted bis(benzyl)phthalic acids using an acid composition comprising trifluoromethanesulfonic acid, the substituted bis(benzyl)phthalic acids being represented b

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