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15828-76-9

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15828-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15828-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,2 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15828-76:
(7*1)+(6*5)+(5*8)+(4*2)+(3*8)+(2*7)+(1*6)=129
129 % 10 = 9
So 15828-76-9 is a valid CAS Registry Number.

15828-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methoxy-4-(4-methoxyphenyl)benzo[f][2]benzofuran-1,3-dione

1.2 Other means of identification

Product number -
Other names 7-Methoxy-1-(4-methoxy-phenyl)-naphthalin-2,3-dicarbonsaeure-anhydrid

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:15828-76-9 SDS

15828-76-9Downstream Products

15828-76-9Relevant articles and documents

One-pot syntheses of blue-luminescent 4-aryl-1H-benzo[f]isoindole-1, 3(2H)-diones by T3P activation of 3-arylpropiolic acids

Deni?en, Melanie,Kraus, Alexander,Reiss, Guido J.,Müller, Thomas J.J.

supporting information, p. 2340 - 2351 (2017/11/16)

In situ activation of 3-arylpropiolic acids with T3P (n-propylphosphonic acid anhydride) initiates a domino reaction furnishing 4-arylnaphtho[2, 3-c]furan-1, 3-diones in excellent yields. Upon employing these anhydrides as reactive intermediates blue-lumi

1-phenyl -2,3-naphthalene carboxylic acid anhydride, and its process for synthesis of derivatives of

-

Paragraph 0013; 0027-0030, (2017/02/24)

The invention discloses a synthesis method of 1-phenyl-2,3-naphthalene dicarboxylic anhydride and derivatives thereof. The synthesis method is used for synthesizing the 1-phenyl-2,3-naphthalene dicarboxylic anhydride compounds under an alkali condition in

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