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Arachidonoyl-N,N-dimethyl amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

45280-17-9

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45280-17-9 Usage

Uses

Arachidonoyl-N,N-dimethyl amide is a cell-cell communication inhibitor.

Check Digit Verification of cas no

The CAS Registry Mumber 45280-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,2,8 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 45280-17:
(7*4)+(6*5)+(5*2)+(4*8)+(3*0)+(2*1)+(1*7)=109
109 % 10 = 9
So 45280-17-9 is a valid CAS Registry Number.

45280-17-9SDS

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 N,N-dimethylicosa-5,8,11,14-tetraenamide

1.2 Other means of identification

Product number -
Other names Arachidonoyl-N,N-dimethyl amide

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:45280-17-9 SDS

45280-17-9Downstream Products

45280-17-9Relevant academic research and scientific papers

A METHOD OF TREATING PERIPHERAL INFLAMMATORY DISEASE

-

Paragraph 0078-0084; 0121-0122, (2016/12/01)

An active for use in the treatment or inhibition of an inflammatory disease associated with over-activation of Toll-like Receptor 4 (TLR4), Toll-like Receptor 2 (TLR2) and Myeloid differentiating protein 88 (Myd88) adaptor-like protein (Mal) while maintaining a subject's ability to respond normally to a pathogen, in which the active is an oleamide or a derivative thereof.

Some features of an SmI2-(Me2N)3P-THF system. Transformation of esters into dimethylamides

Ivanova,Shainurova,Miftakhov

, p. 329 - 331 (2007/10/03)

Sm11-intermediates generated upon addition of (Me2N)3P to a solution of SmI2 in THF exhibit the properties of a single-electron reducing agent and an N-nucleophile. In particular, N,N-dimethylamides are formed from esters.

Arachidonic acid amide inhibitors of gap junction cell-cell communication

Boger, Dale L.,Sato, Haruhiko,Lerner, Aaron E.,Guan, Xiaojun,Gilula, Norton B.

, p. 1151 - 1154 (2007/10/03)

A series of arachidonic acid amides including anandamide and arachidonamide that act as potent inhibitors of the rat glial cell gap junction is described.

Structural requirements for binding of anandamide-type compounds to the brain cannabinoid receptor

Sheskin, Tzviel,Hanu?, Lumir,Slager, Joram,Vogel, Zvi,Mechoulam, Raphael

, p. 659 - 667 (2007/10/03)

In order to establish the structural requirements for binding to the brain cannabinoid receptor (CB1), we have synthesized numerous fatty acid amides, ethanolamides, and some related simple derivatives and have determined their K(i) values. A f

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