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methyl N-benzyl-piperidin-4-yl-cyanoacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

743417-80-3

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743417-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 743417-80-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,3,4,1 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 743417-80:
(8*7)+(7*4)+(6*3)+(5*4)+(4*1)+(3*7)+(2*8)+(1*0)=163
163 % 10 = 3
So 743417-80-3 is a valid CAS Registry Number.

743417-80-3SDS

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 methyl N-benzyl-piperidin-4-yl-cyanoacetate

1.2 Other means of identification

Product number -
Other names -

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:743417-80-3 SDS

743417-80-3Relevant articles and documents

Synthesis and evaluation of tacrine-E2020 hybrids as acetylcholinesterase inhibitors for the treatment of Alzheimer's disease

Shao, Dong,Zou, Chunyan,Luo, Cheng,Tang, Xican,Li, Yuanchao

, p. 4639 - 4642 (2007/10/03)

Tacrine-E2020 hybrids and some related compounds were prepared and their bioactivities on the Alzheimer's Disease were assayed. The optimum hybrid inhibitor 3 is much more potent and selective than tacrine in vitro. Tacrine-E2020 hybrids and some related compounds were prepared and their bioactivities on the Alzheimer's disease were assayed. The optimum hybrid inhibitor 3 is 37-fold more potent and 31-fold more selective than tacrine in vitro.

Synthesis of some new 4-substituted N-benzyl-piperidines

Doernyei, Gabor,Incze, Maria,Moldvai, Istvan,Szantay, Csaba

, p. 2329 - 2338 (2007/10/03)

Via Knoevenagel condensation of N-benzyl-4-piperidone with malononitrile some new 4-substituted N-benzyl-piperidines have been prepared. By means of these transformations an economic and large-scale synthesis of biologically important intermediate N-benzyl-piperidine-4-ethanol has been elaborated.

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