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115170-07-5

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115170-07-5 Usage

General Description

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

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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