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1400742-66-6

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1400742-66-6 Usage

Uses

2-(Pyrrolidin-1-yl)-1-(thiophen-2-yl)pentan-1-one is a stimulant drug. 2-(Pyrrolidin-1-yl)-1-(thiophen-2-yl)pentan-1-one is an analogue of α-Pyrrolidinovalerophenone (α-PVP). α-PVP is a dangerous designer drug and it is being marketed as ‘bath salt’ in the illicit drug market.

Check Digit Verification of cas no

The CAS Registry Mumber 1400742-66-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,0,7,4 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1400742-66:
(9*1)+(8*4)+(7*0)+(6*0)+(5*7)+(4*4)+(3*2)+(2*6)+(1*6)=116
116 % 10 = 6
So 1400742-66-6 is a valid CAS Registry Number.

1400742-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pyrrolidin-1-yl-1-thiophen-2-ylpentan-1-one

1.2 Other means of identification

Product number -
Other names 2-(Pyrrolidin-1-yl)-1-(thiophen-2-yl)pentan-1-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:1400742-66-6 SDS

1400742-66-6Upstream product

1400742-66-6Downstream Products

1400742-66-6Relevant articles and documents

Synthetic method of 2-substituted-1-(2-thiophene)-1-pentanone

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Paragraph 0014; 0015, (2018/03/28)

The invention discloses a synthetic method of 2-substituted-1-(2-thiophene)-1-pentanone. The method includes the steps: taking n-pentanoic acid and bromine as raw materials, and taking phosphorus trichloride as a catalyst to prepare 2-bromovaleric acid; mixing the 2-bromovaleric acid and thionyl chloride to obtain 2-bromovaleryl chloride; taking aluminum trichloride as a catalyst, dropping thiophene into 2-bromovaleryl chloride, and stirring mixture to obtain 2-bromine-1-(2-thiophene)-1-pentanon; performing heating reflux on the 2-bromine-1-(2-thiophene)-1-pentanon and pyrrolidine or piperidine to obtain the 2-substitution-1-(2-thiophene)-1-pentanone. A target compound is a precursor compound for synthesizing drugs such as anticonvulsant drugs or vasodilator drugs and provided with an important pharmaceutical intermediate.