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108781-14-2

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108781-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108781-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,8 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108781-14:
(8*1)+(7*0)+(6*8)+(5*7)+(4*8)+(3*1)+(2*1)+(1*4)=132
132 % 10 = 2
So 108781-14-2 is a valid CAS Registry Number.

108781-14-2SDS

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 3-(4-Methoxybenzyloxy)benzaldehyde

1.2 Other means of identification

Product number -
Other names 3-(p-methoxybenzyloxy)benzaldehyde

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:108781-14-2 SDS

108781-14-2Relevant articles and documents

INHIBITORS OF ANTIGEN PRESENTATION BY HLA-DR

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Paragraph 57-58, (2021/10/11)

Chromanone compounds, pharmaceutical compositions containing them, methods of making them, and methods of using them including methods for treating disease states, disorders, and conditions associated with the inhibition of antigen presentation by HLA-DR.

Irreversible dopamine-β-hydroxylase inhibitors

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, (2008/06/13)

Potent, irreversible dopamine-β-hydroxylase inhibitors having the Formula: STR1 which are useful to inhibit dopamine-β-hydroxylase activity, pharmaceutical compositions including these inhibitors or 2-cyano-2-phenethylamine, and methods of using these inhibitors or 2-cyano-2-phenethylamine to inhibit dopamine-β-hydroxylase activity in mammals. Also disclosed are novel intermediates useful in preparing the presently invented inhibitors.

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