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1796-23-2

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1796-23-2 Usage

Chemical composition

Consists of a piperidine ring and a ketone functional group.

Molecular weight

187.07 g/mol.

Physical state

Colorless liquid.

Boiling point

74-75 °C.

Solubility

Soluble in water.

Uses

Commonly used in organic synthesis as a reagent for the formation of various organic compounds, manufacture of pharmaceuticals and agrochemicals, and as a useful intermediate in the production of fine chemicals.

Safety precautions

Potential irritant to the skin, eyes, and respiratory system. Exposure should be minimized through the use of appropriate personal protective equipment and control measures.

Check Digit Verification of cas no

The CAS Registry Mumber 1796-23-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1796-23:
(6*1)+(5*7)+(4*9)+(3*6)+(2*2)+(1*3)=102
102 % 10 = 2
So 1796-23-2 is a valid CAS Registry Number.

1796-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dichloro-1-piperidin-1-ylethanone

1.2 Other means of identification

Product number -
Other names Dichloressigsaeure-piperidid

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:1796-23-2 SDS

1796-23-2Relevant articles and documents

Dichloromeldrum's acid (DiCMA): A practical and green amine dichloroacetylation reagent

Heard, David M.,Lennox, Alastair J.J.

supporting information, p. 3368 - 3372 (2021/05/06)

Dichloromeldrum's acid is introduced as a bench-stable, nonvolatile reagent for the dichloroacetylation of anilines and alkyl amines to produce α,α-dichloroacetamides, which are important motifs for medicinal chemistry. Products are formed in good to excellent yields with reagent grade solvents, and, as the only byproducts are acetone and CO2, no column chromatography is required. Thus, this reagent is practical, efficient, and green for the dichloroacetylation of primary amines.

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