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4,5-DIMETHOXY-2-NITROCINNAMIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20567-38-8

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20567-38-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20567-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,6 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20567-38:
(7*2)+(6*0)+(5*5)+(4*6)+(3*7)+(2*3)+(1*8)=98
98 % 10 = 8
So 20567-38-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO6/c1-17-9-5-7(3-4-11(13)14)8(12(15)16)6-10(9)18-2/h3-6H,1-2H3,(H,13,14)/p-1/b4-3+

20567-38-8 Well-known Company Product Price

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  • Alfa Aesar

  • (A15824)  4,5-Dimethoxy-2-nitrocinnamic acid, 98%   

  • 20567-38-8

  • 5g

  • 252.0CNY

  • Detail
  • Alfa Aesar

  • (A15824)  4,5-Dimethoxy-2-nitrocinnamic acid, 98%   

  • 20567-38-8

  • 25g

  • 1003.0CNY

  • Detail

20567-38-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-DIMETHOXY-2-NITROCINNAMIC ACID

1.2 Other means of identification

Product number -
Other names RARECHEM BK HW 0176

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:20567-38-8 SDS

20567-38-8Relevant academic research and scientific papers

A Simple and straightforward synthesis of cinnamic acids and ylidene malononitriles via knoevenagel condensation employing dabco as catalyst

Nagalakshmi,Diwakar,Govindh,Gopal Reddy,Venu,Bhargavi,Prasanna Devi,Murthy,Siddaiah

, p. 1561 - 1564 (2017/05/29)

An efficient method for the synthesis of substituted cinnamic acid and ylidene malanonitriles is developed via Knoevenagel condensation of aromatic aldehydes with malonic acid and malononitrile in the presence of catalytic amounts of DABCO. This method has many advantages, such as mild reaction conditions, excellent yields, short reaction times and no furthur purification required.

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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