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84021-19-2

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84021-19-2 Usage

Explanation

This is the systematic name of the compound according to the IUPAC nomenclature system.

Explanation

This is an alternative name for the compound, which is often used in the scientific community.

Explanation

This represents the molecular composition of the compound, indicating the number of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms present.

Explanation

This is the mass of one mole of the compound, calculated based on the atomic weights of its constituent elements.

Explanation

The compound has a unique bicyclic structure, consisting of a six-membered lactam ring fused to a five-membered azabicyclo ring, with an additional hydroxymethylene group attached.

Explanation

The compound contains three main functional groups, which contribute to its reactivity and potential applications.

Explanation

Due to its unique structure, the compound can participate in a range of chemical reactions, making it a valuable building block for the synthesis of new compounds.

Explanation

The compound is commonly used as a starting material for the synthesis of various pharmaceuticals and agrochemicals, thanks to its reactivity and structural features.

Explanation

The compound should be handled with caution due to its potential reactivity and possible health risks. Proper safety measures, such as wearing protective gear and working in a well-ventilated area, should be followed.

Explanation

When working with this compound, it is essential to follow established safety protocols, including the use of appropriate personal protective equipment (PPE) and working in a controlled environment to minimize the risk of exposure or accidents.

Molecular Weight

167.22 g/mol

Structure

Bicyclic with a lactam ring and a hydroxymethylene group

Functional Groups

Lactam, hydroxymethylene, and carbonyl

Reactivity

Potential as a reactive intermediate in various chemical reactions

Applications

Synthetic intermediate in the production of pharmaceuticals and agrochemicals

Hazards

Potential health hazards and reactivity

Safety Precautions

Handle with care and follow safety guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 84021-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,2 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84021-19:
(7*8)+(6*4)+(5*0)+(4*2)+(3*1)+(2*1)+(1*9)=102
102 % 10 = 2
So 84021-19-2 is a valid CAS Registry Number.

84021-19-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxymethylene-3-oxoquinuclidine

1.2 Other means of identification

Product number -
Other names 2-[1-Hydroxy-meth-(E)-ylidene]-1-aza-bicyclo[2.2.2]octan-3-one

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:84021-19-2 SDS

84021-19-2Downstream Products

84021-19-2Relevant articles and documents

SYNTHESIS OF 2-HYDROXYMETHYLENE- AND 2-DIMETHYLAMINOMETHYLENE-3-OXOQUINUCLIDINES AND THEIR REACTIONS WITH NUCLEOPHILIC REAGENTS

Gorbyleva, O. I.,Filipenko, T. Ya.,Mikhlina, E. E.,Turchin, K. F.,Sheinker, Yu. N.,Yakhontov, L. N.

, p. 948 - 954 (2007/10/02)

The reaction of 3-oxoquinuclidine with ethyl formate in the presence of sodium and with dimethylformamide diethylacetal was used to synthesize 2-hydroxymethylene- and 2-dimethylaminomethylene-3-oxoquinuclidines, which upon reaction with amines from N-substituted 2-aminomethylene-3-oxoquinuclidines and upon reaction with hydrazine hydrate give pyrazoloquinuclidines.The reaction of 2-aryl- and 2-heteroarylmethylene-3-oxoquinuclidines with hydrazine hydrate and thiourea, which led to the synthesis of pyrazolo- and pyrimidoquinuclidines with aryl or heteroaryl substituents in the resulting ring, was studied.

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