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[S,(+)]-3-O-Benzyl-1-O,2-O-dimyristoyl-L-glycerol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73083-33-7

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73083-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73083-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,8 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73083-33:
(7*7)+(6*3)+(5*0)+(4*8)+(3*3)+(2*3)+(1*3)=117
117 % 10 = 7
So 73083-33-7 is a valid CAS Registry Number.

73083-33-7SDS

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 1-(tetradecanoyl)-3-O-benzyl-sn-glycerol

1.2 Other means of identification

Product number -
Other names (S)-1-benzyloxy-2,3-bis-myristoyloxy-propane

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:73083-33-7 SDS

73083-33-7Relevant articles and documents

The Chiral Target of Daptomycin Is the 2R,2′S Stereoisomer of Phosphatidylglycerol

Moreira, Ryan,Taylor, Scott D.

, (2021/12/09)

Daptomycin (dap) is an important antibiotic that interacts with the bacterial membrane lipid phosphatidylglycerol (PG) in a calcium-dependent manner. The enantiomer of dap (ent-dap) was synthesized and was found to be 85-fold less active than dap against

HYDROPHOBIC ACID ADDITION SALTS AND PHARMACEUTICAL FORMULATIONS THEREOF

-

Page/Page column 81-82, (2019/05/22)

The invention provides hydrohphobic drug salts and pharmaceutical compositions comprising such salts. The invention fourther provides compositions for delivering poorly soluble drugs, including hydrophobic drug salts.

COMPOSITIONS AND METHODS FOR DELIVERY OF THERAPEUTIC AGENTS

-

, (2017/07/18)

This disclosure provides improved lipid-based compositions, including lipid nanoparticle compositions, and methods of use thereof for delivering agents in vivo including nucleic acids and proteins. These compositions are not subject to accelerated blood clearance and they have an improved toxicity profile in vivo.

Synthesis and structural characterization of three unique helicobacter pylori a-cholesteryl phosphatidyl glucosides

Nguyen, Huy Q.,Davis, Ryan A.,Gervay-Hague, Jacquelyn

supporting information, p. 13400 - 13403 (2015/01/09)

Steryl glycosides produced by bacteria play important biological roles in the evasion and modulation of host immunity. Step-economical syntheses of three cholesteryl-6-Ophosphatidyl-α-d-glucopyranosides (αCPG) unique to Helicobacter pylori have been achie

Synthesis of boron cluster lipids: Closo-dodecaborate as an alternative hydrophilic function of boronated liposomes for neutron capture therapy

Lee, Jong-Dae,Ueno, Manabu,Miyajima, Yusuke,Nakamura, Hiroyuki

, p. 323 - 326 (2008/02/03)

(Chemical Equation Presented) We succeeded in the synthesis of the double-tailed boron cluster lipids 4a-c and 5a-c, which have a B 12H11S moiety as a hydrophilic function, by S-alkylation of B12H11SH (BSH) with bromoacetyl and chloroacetocarbamate derivatives of diacylglycerols for a liposomal boron delivery system on neutron capture therapy. Calcein encapsulation experiments revealed that the liposomes, prepared from the boron cluster lipid 4b, DMPC, PEG-DSPE, and cholesterol, are stable at 37°C in FBS solution for 24 h.

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