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3-(2-Methoxy-5-nitrophenyl)propenoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69447-75-2

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69447-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69447-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,4 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69447-75:
(7*6)+(6*9)+(5*4)+(4*4)+(3*7)+(2*7)+(1*5)=172
172 % 10 = 2
So 69447-75-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO5/c1-16-9-4-3-8(11(14)15)6-7(9)2-5-10(12)13/h2-6H,1H3,(H,12,13)/b5-2+

69447-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(2-methoxy-5-nitrophenyl)prop-2-enoic acid

1.2 Other means of identification

Product number -
Other names 5-nitro-2-methoxy-trans-cinnamic acid

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:69447-75-2 SDS

69447-75-2Relevant academic research and scientific papers

Cerium(IV)-induced nitration of cinnamic acids. Novel remote electrophilic substitution

Peterson, John R.,Do, Hoang D.,Dunham, Andrew J.

, p. 1670 - 1674 (2007/10/02)

The treatment of (E)-3,4-dimethoxycinnamic acid with ceric amonium nitrate in trifluoroacetic acid afforded (E)1,2-dimethoxy-4-nitro-5-(2-nitroethenyl)benzene in 79percent yield.The unusual ipso substitution of the carboxylic acid moiety by a nitro functional center illustrated a new reaction manifold of cerium(IV).Six cinnamic acids were examined to ascertain the generality of the transformation.The bidentate nitrato structure of the metal salt is believed to account for the nitrating ability of this system.

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