2-Arachidonyl Glycerol-d5

Base Information

Chemical Name:2-Arachidonyl Glycerol-d5
CAS No.:1215168-37-8
Molecular Formula:C₂₃H₃₈O₄
Molecular Weight:383.513
Hs Code.:
Mol file:1215168-37-8.mol

Synonyms:2-Arachidonyl Glycerol-d5;(all-Z)-5,8,11,14-Eicosatetraenoic Acid 2-Hydroxy-1- (hydroxyMethyl)ethyl-d5 Ester;2-Monoarachidonoylglycerol-d5;5Z,8Z,11Z,14Z)-5,8,11,14-Eicosatetraenoic Acid 2-Hydroxy-1-(hydroxyMethyl) ethyl-d5 Ester

Suppliers and Price of 2-Arachidonyl Glycerol-d5

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 4 raw suppliers

Chemical Property of 2-Arachidonyl Glycerol-d5

Chemical Property:

PSA：66.76000
LogP:5.02850

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Labelled 2-Arachidonoylglycerol (A765050). It is a major endocannabinoid, which can inhibit synaptic transmission by presynaptic cannabinoid CB1 receptors. It plays an inhibitory role in the bombesin-induced activation of central adrenomedullary outflow in rats.

Technology Process of 2-Arachidonyl Glycerol-d5

There total 1 articles about 2-Arachidonyl Glycerol-d5 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 62502-71-0
[1,1,2,3,3-2H₅]glycerol

: 506-32-1,236743-58-1
all cis 5,8,11,14-eicosatetraenoic acid

: 1215168-37-8
2-arachidonoyl glycerol-d5

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In acetonitrile; at 20 ℃;
DOI:10.1021/ac0624086