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8-[5-(4-fluorophenyl)pentan-2-yl]-5,5-dimethyl-10-(prop-2-en-1-yloxy)-5H-chromeno[4,3-c]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55477-16-2

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55477-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55477-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,7 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55477-16:
(7*5)+(6*5)+(5*4)+(4*7)+(3*7)+(2*1)+(1*6)=142
142 % 10 = 2
So 55477-16-2 is a valid CAS Registry Number.

55477-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-[5-(4-fluorophenyl)pentan-2-yl]-5,5-dimethyl-10-prop-2-enoxychromeno[4,3-c]pyridine

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:55477-16-2 SDS

55477-16-2Downstream Products

55477-16-2Relevant academic research and scientific papers

5H-[1]Benzopyrano[3,4-d]pyridines

-

, (2008/06/13)

5H-[1]Benzopyrano[3,4-d]pyridines represented by the formula STR1 wherein each R1 is loweralkyl, R2 is alkyl, cycloalkyl or STR2 wherein Y is a straight or branched chain alkylene group having from 1 to 10 carbon atoms and each Rsub

Cannabinoids. Synthesis and central nervous system activity of 8 substituted 10 hydroxy 5,5 dimethyl 5H [1]benzopyrano[4,3 c] pyridine and derivatives

Lee,Michaels,Zaugg,Dren,Plotnikoff,Young

, p. 1508 - 1511 (2007/10/05)

8-(1,2-Dimethylheptyl)- and 8-[5-(4-fluorophenyl)-2-pentyl]-10-hydroxy- 5,5-dimethyl-5H-[1]benzopyrano[4,3-c]pyridines (2a and 2b), their phenolic ester and ether derivatives, and their N-oxides were synthesized and evaluated in various CNS pharmacological tests in animals. 2a was found to be the most potent compound.

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