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1-[(2E)-3-(4-fluorophenyl)prop-2-enoyl]-2-methylpiperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105919-40-2

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105919-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105919-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,1 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 105919-40:
(8*1)+(7*0)+(6*5)+(5*9)+(4*1)+(3*9)+(2*4)+(1*0)=122
122 % 10 = 2
So 105919-40-2 is a valid CAS Registry Number.

105919-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(4-fluorophenyl)-1-(2-methylpiperidin-1-yl)prop-2-en-1-one

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:105919-40-2 SDS

105919-40-2Upstream product

105919-40-2Downstream Products

105919-40-2Relevant academic research and scientific papers

Cinnamoyl piperidines and thiomorpholine and cerebral protection compositions

-

, (2008/06/13)

Compounds of the general formula STR1 wherein: X is halogen or trifluoromethyl; R1 is hydrogen, halogen or trifluoromethyl; R2 is hydrogen, methyl or hydroxymethyl; R3 is hydrogen or lower alkyl; and Y is methylene, methylene substituted with a lower alkyl or hydroxyl group, sulfinyl, sulfonyl, oxygen or sulfur, exhibit a cerebral protective effect and are applicable to the treatment of cerebral ischaemia and cerebral hypoxia. The compounds may be made by acylating a suitable piperidine or morpholine with the appropriate cinnamoyl chloride, and if necessary oxidizing the reaction product.

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