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3140-33-8

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3140-33-8 Usage

Type of compound

Organic

Structure

Piperidine skeleton with ethyl and ethanol substituents

Usage

Synthesis of pharmaceuticals and other organic compounds

Key intermediate

In preparation of various drugs (antihistamines, psychotropic drugs)

Application

Building block in the production of other chemical substances

Check Digit Verification of cas no

The CAS Registry Mumber 3140-33-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,4 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3140-33:
(6*3)+(5*1)+(4*4)+(3*0)+(2*3)+(1*3)=48
48 % 10 = 8
So 3140-33-8 is a valid CAS Registry Number.

3140-33-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-piperidyl)-2-butanol

1.2 Other means of identification

Product number -
Other names 1-Piperidino-butanol-(2)

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:3140-33-8 SDS

3140-33-8Downstream Products

3140-33-8Relevant articles and documents

HYDROBORATION OF 1-(3-BUTENYL)PIPERIDINE AND 1-(4-PENTENYL)PIPERIDINE

Kafka, Stanislav,Ferles, Miloslav

, p. 78 - 85 (2007/10/02)

Hydroboration of 1-(3-butenyl)- (Ia) and 1-(4-pentenyl)piperidine (Ib) with triethylamine-borane followed by hydrolysis and oxidation afforded the appropriate alcohols IIIc and IIIf resp.The spirocyclic amine-borane IIa,b isolated from the hydroboration product were transformed by hydrochloric acid into the hydrochlorides of piperidinealkylboronic acids IVa,b which were oxidized in an alkaline medium with hydrogen peroxide to the primary alcohols IIIc,f.Diethyl ester V was prepared by ethanolysis of IIa.

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