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N-Piperidino-α-phenylselenoacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128010-34-4

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128010-34-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128010-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,0,1 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128010-34:
(8*1)+(7*2)+(6*8)+(5*0)+(4*1)+(3*0)+(2*3)+(1*4)=84
84 % 10 = 4
So 128010-34-4 is a valid CAS Registry Number.

128010-34-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Piperidino-α-phenylselenoacetamide

1.2 Other means of identification

Product number -
Other names .selenopiperidide of phenylacetic acid

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:128010-34-4 SDS

128010-34-4Relevant academic research and scientific papers

Copper(0)-induced deselenative insertion of N,N-disubstituted selenoamides into acetylenic C-H bond leading to propargylamines

Mitamura, Takenori,Ogawa, Akiya

supporting information; experimental part, p. 2045 - 2048 (2009/10/24)

Upon heating at 110 °C in the presence of copper(0) powder, terminal acetylenes undergo a novel deselenative C-H bond insertion reaction of N,N-disubstituted selenoamides, affording the corresponding propargylamines in good to excellent yields, selectivel

π-conjugated poly(dithiafulvene)s and poly(diselenafulvene)s: Effects of side alkyl chains on optical, electrochemical, and conducting properties

Naka, Kensuke,Uemura, Takashi,Chujo, Yoshiki

, p. 3539 - 3543 (2007/10/03)

Electron-donating π-conjugated polymers with dithiafulvene moiety (4) or with diselenafulvene moiety (5) were prepared by cycloaddition polymerization of chalcogenoketenes derived from aromatic diynes (3). The solubilities of the polymers strongly depende

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