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15112-62-6

15112-62-6

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15112-62-6 Usage

Chemical Properties

Yellowish brown liquid

Check Digit Verification of cas no

The CAS Registry Mumber 15112-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,1 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15112-62:
(7*1)+(6*5)+(5*1)+(4*1)+(3*2)+(2*6)+(1*2)=66
66 % 10 = 6
So 15112-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H6IN/c1-5-6(7)3-2-4-8-5/h2-4H,1H3

15112-62-6SDS

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 3-Iodo-2-methylpyridine

1.2 Other means of identification

Product number -
Other names 3-iodo-2-methyl-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:15112-62-6 SDS

15112-62-6Upstream product

15112-62-6Downstream Products

15112-62-6Relevant articles and documents

Synthesis and Reactivity of Triazaphenanthrenes

Fernandez, Sarah,Ganiek, Maximilian A.,Karpacheva, Mariia,Hanusch, Fabian C.,Reuter, Stephan,Bein, Thomas,Auras, Florian,Knochel, Paul

supporting information, p. 3158 - 3161 (2016/07/14)

Pyridonaphthyridines (triazaphenanthrenes) were prepared in 4 steps and in 13-52% overall yield using Negishi cross-couplings between iodopicolines and 2-chloro-pyridylzinc derivatives. After chlorination, Gabriel amination and spontaneous ring-closure, the final aromatization leading to the triazaphenanthrenes was achieved with chloranil. This heterocyclic scaffold underwent a nucleophilic addition at position 6 leading to further functionalized pyridonaphthyridines. The influence of these chemical modifications on the optical properties was studied by steady-state and time-resolved optical spectroscopy. While the thiophene-substituted heterocycles exhibited the most extended absorption, the phenyl- and furan-substituted compounds showed a stronger photoluminescence, reaching above 20% quantum yield and lifetimes of several nanoseconds.

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