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N-(3-IODO-PYRIDIN-4-YL)-2,2-DIMETHYL-PROPIONAMIDE is a chemical compound characterized by the molecular formula C12H15IN2O. It is a derivative of 2,2-dimethyl-propionamide, featuring a pyridine ring with an iodine atom at the 3-position. N-(3-IODO-PYRIDIN-4-YL)-2,2-DIMETHYL-PROPIONAMIDE is recognized for its potential in the synthesis of pharmaceuticals and organic compounds, as well as its possible applications in medicinal chemistry and drug development due to its unique structural attributes. Careful handling and adherence to safety protocols are essential to mitigate any health and environmental risks associated with N-(3-IODO-PYRIDIN-4-YL)-2,2-DIMETHYL-PROPIONAMIDE.

113975-33-0

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113975-33-0 Usage

Uses

Used in Pharmaceutical Synthesis:
N-(3-IODO-PYRIDIN-4-YL)-2,2-DIMETHYL-PROPIONAMIDE is utilized as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide range of organic compounds, making it a valuable component in the development of new medications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, N-(3-IODO-PYRIDIN-4-YL)-2,2-DIMETHYL-PROPIONAMIDE is employed for its potential to contribute to the discovery and design of new drugs. Its structural features may offer novel pathways for drug interactions and therapeutic effects.
Used in Drug Development:
N-(3-IODO-PYRIDIN-4-YL)-2,2-DIMETHYL-PROPIONAMIDE plays a role in drug development, where its properties can be harnessed to improve the efficacy and safety of new pharmaceutical agents. Its presence in the synthesis process can lead to the creation of compounds with specific therapeutic targets.
Used in Chemical Research:
N-(3-IODO-PYRIDIN-4-YL)-2,2-DIMETHYL-PROPIONAMIDE is also used in chemical research to explore new reactions and bonding mechanisms, potentially leading to advancements in organic chemistry and related fields.
Used in Environmental and Health Safety Protocols:
While not an application in the traditional sense, the need for proper handling and safety measures when working with N-(3-IODO-PYRIDIN-4-YL)-2,2-DIMETHYL-PROPIONAMIDE is crucial. It is used to ensure the protection of both the environment and individuals involved in its synthesis and application processes.

Check Digit Verification of cas no

The CAS Registry Mumber 113975-33-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,9,7 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113975-33:
(8*1)+(7*1)+(6*3)+(5*9)+(4*7)+(3*5)+(2*3)+(1*3)=130
130 % 10 = 0
So 113975-33-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H13IN2O/c1-10(2,3)9(14)13-8-4-5-12-6-7(8)11/h4-6H,1-3H3,(H,12,13,14)

113975-33-0 Well-known Company Product Price

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  • CAS number
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  • Alfa Aesar

  • (H50026)  3-Iodo-4-(2,2,2-trimethylacetamido)pyridine   

  • 113975-33-0

  • 1g

  • 2207.0CNY

  • Detail
  • Alfa Aesar

  • (H50026)  3-Iodo-4-(2,2,2-trimethylacetamido)pyridine   

  • 113975-33-0

  • 5g

  • 9940.0CNY

  • Detail
  • Aldrich

  • (ADE000274)  N-(3-Iodo-pyridin-4-yl)-2,2-dimethyl-propionamide  AldrichCPR

  • 113975-33-0

  • ADE000274-1G

  • 1,611.09CNY

  • Detail

113975-33-0SDS

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 N-(3-IODO-PYRIDIN-4-YL)-2,2-DIMETHYL-PROPIONAMIDE

1.2 Other means of identification

Product number -
Other names N-(3-Iodo-pyridin-4-yl)-2,2-dimethyl-propionamide

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:113975-33-0 SDS

113975-33-0Upstream product

113975-33-0Relevant academic research and scientific papers

Metalation/SRN1 Coupling in Heterocyclic Synthesis. A Convenient Methodology for Ring Functionalization

Estel, L.,Marsais, F.,Queguiner, G.

, p. 2740 - 2744 (1988)

Lithiation, iodination, and fluorine substitution on 2-fluoropyridine gave 2-substituted 3-iodopyridines, which were further subjected to iodine SRN1 substitution by carbon, sulfur, and phosphorus nucleophiles.Iodine substitution by enolates on 2-amino-3-iodopyridines afforded ketones, which were further cyclized to various 1,2-disubstituted pyrrolopyridines. 2-Amino-3-iodo-, 3-amino-4-iodo, and 4-amino-3-iodopyridines were prepared by directed metalation of 2-, 3-, and 4-(pivaloylamino)pyridines.Substitution of iodine by enolates under SRN1 conditions and acidic cyclization led to various 2-substituted pyrrolo, --, and -pyridines in high yields.

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