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56897-45-1

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56897-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56897-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,9 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56897-45:
(7*5)+(6*6)+(5*8)+(4*9)+(3*7)+(2*4)+(1*5)=181
181 % 10 = 1
So 56897-45-1 is a valid CAS Registry Number.

56897-45-1SDS

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 4-bromo-5-methoxy-2-nitro-1-benzofuran

1.2 Other means of identification

Product number -
Other names 4-Bromo-5-methoxy-2-nitrobenzofuran

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:56897-45-1 SDS

56897-45-1Downstream Products

56897-45-1Relevant articles and documents

Sur l'orientation et les anomalies de l'acetylation des Bz-methoxy nitro-2 benzofurannes (1)

Clavel, Jean-Marc,Guillaumel, Jean,Demerseman, Pierre,Royer, Rene

, p. 279 - 283 (2007/10/02)

4-Methoxy-, 5-methoxy- and 7-methoxy-2-nitrobenzofurans have been acetylated via the Friedel-Crafts reaction under the same reaction conditions. 2-Nitrobenzofuran does not undergo acetylation while 6-methoxy-2-nitrobenzofuran only produces decomposition products.As a result of the positive acetylation reactions, 7-acetyl-4-methoxy-, 4-acetyl-5-methoxy- and 4-acetyl-7-methoxy-2-nitrobenzofuran have been prepared.As side products in the acetylation reactions, 4-methoxy-3-(4'-methoxy-2'-nitro-7'-benzofuranyl)-2,3-dihydrobenzofuran-2-one was isolated when 4-methoxy-2-nitrobenzofuran was the starting material and, likewise, when 5-methoxy-2-nitrobenzofuran was the starting material, 3-chloro-5-methoxy-2,3-dihydrobenzofuran-2-one was obtained.Furthermore, 5-methoxy-2-nitrobenzofuran participated in an unexpected chlorination leading to 4-chloro-5-methoxy-2-nitrobenzofuran.

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