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206182-51-6

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206182-51-6 Usage

Physical appearance

White to light yellow solid at room temperature

Solubility

Soluble in water and ethanol

Chemical classification

Derivative of piperidine (a six-membered heterocyclic amine)

Uses

Reagent in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals; versatile building block for the synthesis of various heterocyclic compounds; precursor in the production of other chemical compounds

Hazards

Corrosive and toxic; should be handled with care and stored in a tightly sealed container in a well-ventilated area.

Check Digit Verification of cas no

The CAS Registry Mumber 206182-51-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,1,8 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 206182-51:
(8*2)+(7*0)+(6*6)+(5*1)+(4*8)+(3*2)+(2*5)+(1*1)=106
106 % 10 = 6
So 206182-51-6 is a valid CAS Registry Number.

206182-51-6SDS

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 4-oxopiperidine-1-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 4-oxo-piperidine-1-carbonyl chloride

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:206182-51-6 SDS

206182-51-6Downstream Products

206182-51-6Relevant articles and documents

Use of triphosgene for direct preparation of carbamoyl chlorides from tertiary benzylamines

Jorand-Lebrun, Catherine,Valognes, Delphine,Halazy, Serge

, p. 1189 - 1195 (1998)

A general method for direct preparation of carbamoyl chlorides from corresponding benzylamines using triphosgene is described.

Selective cleavage of N-benzyl-protected secondary amines by triphosgene

Banwell, Martin G.,Coster, Mark J.,Harvey, Michael J.,Moraes, John

, p. 613 - 616 (2007/10/03)

A series of competition experiments has revealed that selective cleavage of N-benzyl-protected secondary amines can be achieved with triphosgene, thereby providing a useful range of carbamoyl chlorides.

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