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2-Propenenitrile,3-(4-pyridinyl)-,(Z)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

123293-75-4

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123293-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123293-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,2,9 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 123293-75:
(8*1)+(7*2)+(6*3)+(5*2)+(4*9)+(3*3)+(2*7)+(1*5)=114
114 % 10 = 4
So 123293-75-4 is a valid CAS Registry Number.

123293-75-4SDS

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 (Z)-3-(4-pyridyl)acrylonitrile

1.2 Other means of identification

Product number -
Other names Z-3-(pyridin-4-yl)acrylonitrile

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:123293-75-4 SDS

123293-75-4Downstream Products

123293-75-4Relevant academic research and scientific papers

Synthesis of olefins via a Wittig reaction mediated by triphenylarsine

Li, Lun,Stimac, Jared C.,Geary, Laina M.

supporting information, p. 1379 - 1381 (2017/03/17)

An arsine-mediated Wittig reaction for the synthesis of olefins is described. After heating triphenylarsine in the presence of an activated alkyl bromide for 30?min, the resulting arsonium salt condensed with aldehydes in as little as 5?min at room temperature, yielding the olefins in high yields. Aromatic, heteroaromatic, and alkyl aldehydes were all suitable substrates for this process.

5, 7-SUBSTITUTED-IMIDAZO [1, 2-C] PYRIMIDINES AS INHIBITORS OF JAK KINASES

-

Page/Page column 79, (2011/11/01)

Compounds of Formula I: (Formula should be inserted here) and stereoisomers and pharmaceutically acceptable salts and solvates thereof in which R1, R2, R3, R4, R5, R6, R7, X1 and X2 have the meanings given in the specification, are inhibitors of one or more JAK kinases and are useful in the treatment of autoimmune diseases, inflammatory diseases, rejection of transplanted organs, tissues and cells, as well as hematologic disorders and malignancies and their co-morbidities.

Efficient synthesis of pyridylacrylonitriles via the Heck reaction

Mei, Kui,Wang, Junbo,Hu, Xianming

, p. 2525 - 2532 (2007/10/03)

A new synthetic pathway to pyridylacrylonitriles has been developed based on a palladium-catalyzed Heck reaction. The optimized process and the preparation of related functionalized pyridylacrylonitriles are discussed. Copyright Taylor & Francis Group, LLC.

Replacement Substituent Constants for Simple Heterocycles

Robinson, Charles N.,Wiseman, Leonard J. Jr.,Slater, Carl D.

, p. 4103 - 4112 (2007/10/02)

13C nmr absorptions are reported for the β-vinylic carbon atoms in 15 series of ethylenes bearing heterocyclic substituents.The data are used to establish the best single-parameter substituent constants, ?13, for the various heterocycles as replacements for para-substituted benzenes.Also reported are replacement dual substituent constants, including ?I and the various ?R scales needed in the Taft DSP treatment and those for F and R used in the Swain-Lupton treatment.Values of ?13, F, R, ?I, and ?Ro, respectively, for the various heterocycles as replacements for para-substituted benzenes are as follows: 2-furyl, -1.01 , 0.99, -2.51, 0.65, -0.60; 2-pyrryl, -2.53, 0.52, -5.09, -0.16, -0.62; 2-thienyl, -0.79, 2.49, -3.60, 1.82, -1.08; 3-thienyl, -0.40, 1.04, -1.57, 0.59, -0.39; 2-pyridyl, 0.88, 2.09, -0.24, 1.65, -0.45; 3-pyridyl, 0.60, 0.57, 0.63, 0.35, 0.04; and 4-pyridyl, 1.18, 1.22, 1.09, 0.92, -0.01.The DSP-NLR method of analysis is explored using electron demand parameters, ε, as determined for the vinylic side chains in para-substituted styrenes.

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