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CAS

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115170-07-5

2-Iodo-3-methoxy-6-nitropyridine is a chemical compound with the molecular formula C6H5IN2O3, belonging to the class of organic compounds known as nitropyridines. It is a derivative of pyridine, featuring a nitro group, an iodo group, and a methoxy group attached to a pyridine ring. This yellow solid at room temperature is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and as a reagent in organic chemistry for creating other compounds. It is stored and handled under strict safety and environmental regulations.

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  • 115170-07-5 Structure

  • Basic information

    1. Product Name: 2-Iodo-3-methoxy-6-nitropyridine
    2. Synonyms: 2-Iodo-3-methoxy-6-nitropyridine
    3. CAS NO:115170-07-5
    4. Molecular Formula: C6H5IN2O3
    5. Molecular Weight: 280.02
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115170-07-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Iodo-3-methoxy-6-nitropyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Iodo-3-methoxy-6-nitropyridine(115170-07-5)
    11. EPA Substance Registry System: 2-Iodo-3-methoxy-6-nitropyridine(115170-07-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 115170-07-5(Hazardous Substances Data)

115170-07-5 Usage

Uses

Used in Pharmaceutical Industry:
2-Iodo-3-methoxy-6-nitropyridine is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure allows for the creation of diverse chemical entities with potential medicinal properties.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Iodo-3-methoxy-6-nitropyridine serves as an intermediate in the production of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds, thereby improving crop yields and quality.
Used in Organic Chemistry Research:
2-Iodo-3-methoxy-6-nitropyridine is utilized as a reagent in organic chemistry for the synthesis of other compounds. Its presence in reactions can facilitate the formation of desired products, enabling researchers to explore new chemical pathways and develop innovative synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 115170-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,7 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 115170-07:
(8*1)+(7*1)+(6*5)+(5*1)+(4*7)+(3*0)+(2*0)+(1*7)=85
85 % 10 = 5
So 115170-07-5 is a valid CAS Registry Number.

115170-07-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Iodo-3-methoxy-6-nitropyridine

1.2 Other means of identification

Product number -
Other names 2-iodanyl-3-methoxy-6-nitro-pyridine

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:115170-07-5 SDS

115170-07-5Downstream Products

115170-07-5Relevant articles and documents

Notiz zur chemischen Reaktivitaet von hydroxylierten Pyridinen

Dehmlow, Eckehard V.,Schulz, Hans-Joachim

, p. 2951 - 2973 (2007/10/02)

Ueber mehrere Schritte werden Maltol in 3,4-Dimethoxy-2-methylpyridin (2b) und Kojisaeure in 3-Brom-4-hydroxy-5-methoxypyridin ueberfuehrt.Die Bromierung von 3,3'-Dihydroxy-2,2'-bipyridin (6) liefert ein Gemisch von Monobrom-, Dibrom-, Tribrom- und Tetrabromverbindungen 7a bis 7g, bei denen die 6-Bromderivate vorherrschen.Aehnliche Substitutionsmuster werden bei der Nitrierung von 6 erhalten, wobei die Verbindungen 7h - 7j erhalten werden.Ausgehend von 2-Iod-3-methoxypyridin (8) lassen sich die Substitutionsprodukte 10 bis 15 darstellen.Als besonders interessant erweist sich 3-Methoxy-2-iod-6-nitropyridin (11), das sich zu dem 3,3',6,6'-Tetrahydroxy-2,2'-bipyridin (16d) umwandeln laesst, einen Isomeren des Naturstoffs Orellin.

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