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6994-14-5

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6994-14-5 Usage

General Description

N-(1-Oxidopyridin-2-yl)acetamide is a chemical compound with the molecular formula C7H7N2O2. It is also known by the synonyms 2-(1-pyridyl)acetamide N-oxide and N-pyridyl-N'-acetamide. N-(1-Oxidopyridin-2-yl)acetamide is an amide derivative of 2-pyridinecarboxylic acid, and it is commonly used as an intermediate in organic synthesis. It is a white to off-white solid and is soluble in organic solvents such as methanol and dichloromethane. N-(1-Oxidopyridin-2-yl)acetamide is often used in pharmaceutical research and manufacturing as a building block for the synthesis of various bioactive compounds. It is also used in the synthesis of heterocyclic compounds and in the production of agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 6994-14-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,9 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6994-14:
(6*6)+(5*9)+(4*9)+(3*4)+(2*1)+(1*4)=135
135 % 10 = 5
So 6994-14-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2/c1-6(10)8-7-4-2-3-5-9(7)11/h2-5,11H,1H3/b8-7+

6994-14-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1-hydroxypyridin-2-ylidene)acetamide

1.2 Other means of identification

Product number -
Other names N-(1-oxy-pyridin-2-yl)-acetamide

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:6994-14-5 SDS

6994-14-5Relevant articles and documents

A new transformation of aminopyridines upon diazotization in acetonitrile with the formation of N-pyridinylacetamides

Chudinov,Dovbnya,Krasnokutskaya,Ogorodnikov,Filimonova

, p. 2312 - 2314 (2017/05/12)

Diazotization of aminopyridines upon treatment with NaNO2 and H3PO4 in acetonitrile led to the formation of N-pyridinylacetamides. This reaction constitutes a convenient and general preparative method for the synthesis of 2-, 3-, and 4-N-pyridinylacetamides under mild conditions in good yields. The in situ oxidation of the thus obtained N-pyridinylacetamides with hydrogen peroxide gave good yields of pyridinylacetamide N-oxides.

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