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2-IODO-ISONICOTINIC ACID METHYL ESTER is a chemical compound with the molecular formula C7H6INO2. It is a derivative of isonicotinic acid and contains an iodine atom, which makes it useful for various chemical reactions and as a building block for the synthesis of more complex molecules. Its methyl ester group also enhances its solubility and stability, making it a versatile and valuable compound for research and development in the fields of chemistry and pharmaceuticals.

134579-47-8

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134579-47-8 Usage

Uses

Used in Organic Synthesis:
2-IODO-ISONICOTINIC ACID METHYL ESTER is used as a building block for the synthesis of more complex molecules, contributing to the development of new chemical compounds.
Used in Pharmaceutical Research:
2-IODO-ISONICOTINIC ACID METHYL ESTER is used as a research compound for exploring its potential applications in the pharmaceutical industry, including its unique properties that may lead to the discovery of new drugs or therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 134579-47-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,5,7 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134579-47:
(8*1)+(7*3)+(6*4)+(5*5)+(4*7)+(3*9)+(2*4)+(1*7)=148
148 % 10 = 8
So 134579-47-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H6INO2/c1-11-7(10)5-2-3-9-6(8)4-5/h2-4H,1H3

134579-47-8 Well-known Company Product Price

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  • Aldrich

  • (ADE000319)  2-Iodo-isonicotinic acid methyl ester  AldrichCPR

  • 134579-47-8

  • ADE000319-1G

  • 4,512.69CNY

  • Detail

134579-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Iodo-isonicotinic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl 2-iodopyridine-4-carboxylate

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:134579-47-8 SDS

134579-47-8Relevant academic research and scientific papers

Efficient copper-catalyzed trifluoromethylation of aromatic and heteroaromatic iodides: The beneficial anchoring effect of borates

Gonda, Zsombor,Kovacs, Szabolcs,Weber, Csaba,Gati, Tamas,Meszaros, Attila,Kotschy, Andras,Novak, Zoltan

supporting information, p. 4268 - 4271 (2014/09/30)

Efficient copper-catalyzed trifluoromethylation of aromatic iodides was achieved with TMSCF3 in the presence of trimethylborate. The Lewis acid was used to anchor the in situ generated trifluoromethyl anion and suppress its rapid decomposition. Broad applicability of the new trifluoromethylating reaction was demonstrated in the functionalization of different aromatic and heteroaromatic iodides.

Aryl-4-ethynyl-isoxazole derivatives

-

Page/Page column 9, (2008/06/13)

The present invention is concerned with aryl-4-ethynyl-isoxazole derivatives of formula I wherein R1 to R5 are as described in the specification and pharmaceutically acceptable salt thereof. This class of compounds has high affinity and selectivity for GABA A α5 receptor binding sites, being useful as a cognitive enhancer or for the treatment of cognitive disorders like Alzheimer's disease.

Imidazole derivatives

-

, (2008/06/13)

Novel imidazole derivatives are disclosed. These compounds have a good affinity to the NMDA (N-methyl-D-aspartate)-receptor subtype selective blockers, which have a key function in modulating neuronal activity and plasticity which makes them key players in mediating processes underlying development of CNS as well as learning and memory formation. These compounds are useful in the control or treatment of diseases mediated by this receptor.

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