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N-HYDROXY-1-OXY-PYRIDINE-2-CARBOXAMIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65370-37-8

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65370-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65370-37-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,7 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65370-37:
(7*6)+(6*5)+(5*3)+(4*7)+(3*0)+(2*3)+(1*7)=128
128 % 10 = 8
So 65370-37-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N3O2/c7-6(8-10)5-3-1-2-4-9(5)11/h1-4,11H,7H2/b6-5-

65370-37-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-hydroxypyridine-2-carboximidamide 1-oxide

1.2 Other means of identification

Product number -
Other names PYRIDINE-2-CARBOXAMIDOXIME N-OXIDE

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:65370-37-8 SDS

65370-37-8Upstream product

65370-37-8Downstream Products

65370-37-8Relevant academic research and scientific papers

Convenient entry to N-pyridinylureas with pharmaceutically privileged oxadiazole substituents via the acid-catalyzed C[sbnd]H activation of N-oxides

Geyl, Kirill,Baykov, Sergey,Tarasenko, Marina,Zelenkov, Lev E.,Matveevskaya, Vladislava,Boyarskiy, Vadim P.

supporting information, (2019/09/12)

Pyridine-N-oxides bearing a pharmacophoric oxadiazole moiety could be C[sbnd]H functionalized via the acid-catalyzed reaction with dialkylcyanamides, providing access to hitherto undescribed pyridine-2-yl substituted ureas, which have potential as “lead-l

Reaction of N-alkylpyridinium salts with hydroxylamine

M?hrle, Hans,Nie?en, Robert

, p. 434 - 442 (2007/10/03)

1-Methylpyridinium salts showed no reaction with excessive hydroxylamine, but nicotinic acid derivatives in HMPT gave the corresponding N-oxides. 3-Acetyl-1-methylpyridinium iodide generated the hydroximino-pyridine 1-oxide 13 and the isoxazoles 14, 15E,

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