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43152-93-8

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43152-93-8 Usage

Type of compound

Cyclic ketone

Usage

Building block in the synthesis of pharmaceuticals and agrochemicals

Physical state

Clear, colorless liquid

Odor

Distinct

Solubility

Soluble in organic solvents such as ethanol, ether, and chloroform

Applications

Intermediate in the production of various drugs, manufacturing of other organic compounds, fragrance and flavor industry

Safety precautions

Harmful if ingested or inhaled, may cause skin and eye irritation, should be handled with caution

Check Digit Verification of cas no

The CAS Registry Mumber 43152-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,5 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 43152-93:
(7*4)+(6*3)+(5*1)+(4*5)+(3*2)+(2*9)+(1*3)=98
98 % 10 = 8
So 43152-93-8 is a valid CAS Registry Number.

43152-93-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ETHYLPIPERIDIN-3-ONE

1.2 Other means of identification

Product number -
Other names 3-Piperidinone,1-ethyl

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:43152-93-8 SDS

43152-93-8Relevant articles and documents

Lightening Agents and/or Dyes that Contain Aldehyde(s)

-

, (2010/12/29)

Agents for dyeing and/or lightening keratin fibers, in particular human hair, containing, relative to the weight thereof, 0.001 to 15 wt. % of at least one aldehyde of the formula (I): wherein X represents —CH(R2)—SO2—Y—R1, —CR3R4R5, or wherein Y represents —CH(CHO)— or —CH2— or a chemical bond, and wherein each of R1, R2, R3, R4, R5, R6, R7, R8, R9, and R10 independently represents —H or —CN or —F or —Cl or —Br or —I or —CHO or —NH2 or —NO2 or —CF3 or —CCl3 or —CF2CF3 or —CCl2CCl3 or an optionally substituted (C1-C6) alkyl group or a hydroxyalkyl group or a polyhydroxyalkyl group or an optionally substituted (C1-C6) alkylene group, and wherein the agent contains no oxidation dye precursors of developer and coupler type.

NITROGENOUS CYCLIC KETONE DERIVATIVE, PROCESS FOR PRODUCING THE SAME, AND USE

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Page 30, (2010/02/08)

A novel compound represented by the formula (I): wherein rings A and B each represents an optionally substituted aromatic ring, or rings A and B may be bonded to each other through linking between bonds or substituents thereof to form a ring; ring C represents a nitrogenous saturated heterocycle optionally having one or more substituents besides the oxo (provided that 2,3-dioxopyrrolidine ring is excluded); R1 represents hydrogen, an optionally substituted hydrocarbon group, or an optionally substituted heterocyclic group; and-------- indicates a single bond or a double bond. It has high antagonistic activity against a tachykinin receptor, especially an SP receptor.

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