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2-Propanol, 1-(octadecyloxy)-3-(triphenylmethoxy)-, (S)- is a complex organic compound with the chemical formula C43H58O3. It is a chiral molecule, with the (S)-configuration indicating the spatial arrangement of its atoms. 2-Propanol, 1-(octadecyloxy)-3-(triphenylmethoxy)-, (S)- is characterized by a 2-propanol backbone, which is a three-carbon alcohol, with an octadecyloxy group attached to the first carbon and a triphenylmethoxy group attached to the third carbon. The octadecyloxy group consists of an 18-carbon alkyl chain, while the triphenylmethoxy group features three phenyl rings attached to an oxygen atom. 2-Propanol, 1-(octadecyloxy)-3-(triphenylmethoxy)-, (S)- is likely to be used in specialized applications due to its unique structure, such as in the synthesis of certain pharmaceuticals or as a component in specific chemical reactions.

6076-32-0

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6076-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6076-32-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,7 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6076-32:
(6*6)+(5*0)+(4*7)+(3*6)+(2*3)+(1*2)=90
90 % 10 = 0
So 6076-32-0 is a valid CAS Registry Number.

6076-32-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-O-trityl-3-O-octadecyl-sn-glycerol

1.2 Other means of identification

Product number -
Other names 1-O-octadecyl-3-O-trityl-glycerol

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:6076-32-0 SDS

6076-32-0Relevant academic research and scientific papers

D and L etherlipid stereoisomers and liposomes

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Page column 12, (2008/06/13)

A liposome having a lipid bilayer, where the lipid bilayer includes either the L or D stereoisomer of an ether lipid or a non-equal mixture of both. Most preferably the liposome also comprises (a) an underivatized phosphatidylcholine; (b) a sterol; (c) about 5-20 mole % of a phosphatidylethanolamine linked to a dicarboxylic acid at the ethanolamine group of the phosphatidylethanolamine, and (d) greater than about 10 mole % to less than about 30 mole % of either the L or D stereoisomer of an ether lipid. The liposome may be used as an anti-cancer or anti-inflammatory agent.

Synthesis of glyceryl ethers in high optical purity via ruthenium catalyzed asymmetric hydrogenation

Cesarotti, Edoardo,Mauri, Angela,Pallavicini, Marco,Villa, Luigi

, p. 4381 - 4384 (2007/10/02)

1-O-octadecyl-3-O-trityl-glycerol and 1-O-benzyl-3-O-trityl-glycerol can be prepared by asymmetric catalytic hydrogenation in O.P.> 96% and 87-88% respectively.

Stereoselective Synthesis of Long-chain 1-O-(β-D-Maltosyl)-3-O-alkyl-sn-glycerols (Alkyl Glyceryl Ether Lysoglycolipids)

Prinz, Harald,Six, Lambert,Ruess, Klaus-Peter,Lieflaender, Manfred

, p. 217 - 225 (2007/10/02)

The synthesis of long-chain 2-O-benzyl-3-O-alkyl-sn-glycerols 5 was improved, making these compounds easily accessible for glycosylation experiments.Glycosylation with α-acetobromomaltose following a modified Koenings-Knorr procedure after removal of the protective groups yielded the title compound 9 in good yields.These compounds represent examples of alkyl glyceryl ether lysoglycolipids.Some properties of these amphiphilic compounds with a nonionic carbohydrate head-group differ not much (critical micell concentration, hemolytic activity), other properties differ very much (antitumor efficiency) from the properties of the analogous compounds with a zwitterionic phosphorylcholine head-group.

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