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38749-96-1

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38749-96-1 Usage

Uses

3-Iodo-4-methylpyridine is used as a reactant in the preparation of 7a-heteroarylhexahydro-1H-pyrrolizines as cholinergic synaptic transmission modulators.

Check Digit Verification of cas no

The CAS Registry Mumber 38749-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,4 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38749-96:
(7*3)+(6*8)+(5*7)+(4*4)+(3*9)+(2*9)+(1*6)=171
171 % 10 = 1
So 38749-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H6IN/c1-5-2-3-8-4-6(5)7/h2-4H,1H3

38749-96-1SDS

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 3-iodo-4-methylpyridine

1.2 Other means of identification

Product number -
Other names 3-Jod-4-methyl-pyridin

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:38749-96-1 SDS

38749-96-1Relevant articles and documents

Anti-Markovnikov Hydroarylation of Unactivated Olefins via Pyridyl Radical Intermediates

Boyington, Allyson J.,Riu, Martin-Louis Y.,Jui, Nathan T.

supporting information, p. 6582 - 6585 (2017/05/29)

The intermolecular alkylation of pyridine units with simple alkenes has been achieved via a photoredox radical mechanism. This process occurs with complete regiocontrol, where single-electron reduction of halogenated pyridines regiospecifically yields the corresponding radicals in a programmed fashion, and radical addition to alkene substrates occurs with exclusive anti-Markovnikov selectivity. This system is mild, tolerant of many functional groups, and effective for the preparation of a wide range of complex alkylpyridines.

Preparation of 7a-heteroarylhexahydro-1H-pyrrolizines as cholinergic synaptic transmission modulators.

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, (2008/06/13)

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