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N-(1,1-Dimethylethyl)-3-iodo-4-pyridinecarboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

331969-21-2

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331969-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 331969-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,9,6 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 331969-21:
(8*3)+(7*3)+(6*1)+(5*9)+(4*6)+(3*9)+(2*2)+(1*1)=152
152 % 10 = 2
So 331969-21-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13IN2O/c1-10(2,3)13-9(14)7-4-5-12-6-8(7)11/h4-6H,1-3H3,(H,13,14)

331969-21-2SDS

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-tert-butyl-3-iodopyridine-4-carboxamide

1.2 Other means of identification

Product number -
Other names -

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:331969-21-2 SDS

331969-21-2Downstream Products

331969-21-2Relevant academic research and scientific papers

Deprotonation of pyridine carboxamides using lithium magnesiates bases

Hawad, Ha?an,Bayh, Omar,Hoarau, Christophe,Trécourt, Francois,Quéguiner, Guy,Marsais, Francis

, p. 3236 - 3245 (2008/09/21)

Regioselective deprotonation of N-methyl- and tert-butylpyridine carboxamides using lithium magnesiates bases was achieved at room temperature avoiding nucleophilic addition on the pyridine molecule and auto-condensation of the arylmetal intermediates on

Reaction of magnesiated bases on substituted pyridines: Deprotonation or 1,4-addition?

Bonnet, Veronique,Mongin, Florence,Trecourt, Francois,Queguiner, Guy

, p. 4245 - 4249 (2007/10/03)

N-(tert-Butyl)pyridine-2-carboxamide (1), N-phenylpyridine-2-carboxamide (7) and 2,2-dimethyl-N-(2-pyridyl)-propanamide (18) are readily deprotonated at C3 with a stoichiometric amount of PriMgCl or Bu2Mg in THF under reflux. Subsequ

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