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34023-62-6

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34023-62-6 Usage

Uses

1-BCP is a centrally active selective potentiator of AMPA-mediated responses.

Biological Activity

A centrally active selective potentiator of AMPA-mediated responses. Facilitates memory retention in rats.

Check Digit Verification of cas no

The CAS Registry Mumber 34023-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,0,2 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34023-62:
(7*3)+(6*4)+(5*0)+(4*2)+(3*3)+(2*6)+(1*2)=76
76 % 10 = 6
So 34023-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO3/c15-13(14-6-2-1-3-7-14)10-4-5-11-12(8-10)17-9-16-11/h4-5,8H,1-3,6-7,9H2

34023-62-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-benzodioxol-5-yl(piperidin-1-yl)methanone

1.2 Other means of identification

Product number -
Other names 1-BCP

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:34023-62-6 SDS

34023-62-6Relevant academic research and scientific papers

Direct Synthesis of Enamides via Electrophilic Activation of Amides

Berger, Martin,Kaiser, Daniel,Maulide, Nuno,Spie?, Philipp

supporting information, p. 10524 - 10529 (2021/07/28)

A novel, one-step N-dehydrogenation of amides to enamides is reported. This reaction employs the unlikely combination of LiHMDS and triflic anhydride, which serves as both the electrophilic activator and the oxidant, and is characterized by its simple setup and broad substrate scope. The synthetic utility of the formed enamides was readily demonstrated in a range of downstream transformations.

Synthesis, crystal structure and anti-fatigue effects of some benzamide derivatives

Wu, Xianglong,Fan, Wutu,Pan, Yalei,Zhai, Yuankun,Niu, Yinbo,Li, Chenrui,Mei, Qibing

, p. 1034 - 1046 (2014/02/14)

A series of benzamide derivatives such as 1-(1,3-benzodioxol-5-ylcarbonyl) piperidine (1-BCP) were synthesized by the reaction of substituted benzoic acids with piperidine, morpholine or pyrrolidine using a novel method. The crystals of these benzamide de

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