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(2R)-3-[(hydroxy{[(2R,3R,5S,6R)-2,3,5,6-tetrahydroxy-4-(phosphonooxy)cyclohexyl]oxy}phosphoryl)oxy]propane-1,2-diyl dihexadecanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57606-15-2

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57606-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57606-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,0 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57606-15:
(7*5)+(6*7)+(5*6)+(4*0)+(3*6)+(2*1)+(1*5)=132
132 % 10 = 2
So 57606-15-2 is a valid CAS Registry Number.

57606-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R)-2-hexadecanoyloxy-3-[hydroxy-[(2R,3R,5S,6R)-2,3,5,6-tetrahydroxy-4-phosphonooxycyclohexyl]oxyphosphoryl]oxypropyl] hexadecanoate

1.2 Other means of identification

Product number -
Other names oxy]propane-1,2-diyl dihexadecanoate

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:57606-15-2 SDS

57606-15-2Downstream Products

57606-15-2Relevant academic research and scientific papers

Comprehensive and uniform synthesis of all naturally occurring phosphorylated phosphatidylinositols

Kubiak, Robert J.,Bruzik, Karol S.

, p. 960 - 968 (2007/10/03)

Studies of cellular signal transduction mechanisms involving receptor-mediated generation of inositol phosphates and phosphorylated phosphatidylinositols require easy access to these naturally occurring products. Although numerous synthetic methods have been developed during the past decade, most of these methods suffer from excessive length and lack of generality. In this work we describe the comprehensive and uniform synthesis of all naturally occurring phosphatidylinositols such as phosphatidylinositol, phosphatidylinositol 3-phosphate, 4-phosphate, 5-phosphate, 3,4-bisphosphate, 3,5-bisphosphate, 4,5-bisphosphate, and 3,4,5-trisphosphate, featuring both saturated and unsaturated fatty acid chains.

Comparison of cyclic and acyclic phosphites by selective phosphorylation. Synthesis of phosphatidylinositol 4-phosphate

Watanabe, Yutaka,Munetsugu, Hirofumi,Hayashi, Minoru

, p. 292 - 293 (2007/10/03)

To compare the synthetic utility of cyclic xylylene N,N-diethylphosphoramidite and its acyclic analog, dibenzyl ester, both phosphites derived from them with dipalmitoylglycerol were subjected to the selective phosphorylation at the OH-3 position in 1,2:4

IMPROVED SYNThESES OF INOSITOL PHOSPHOLIPID ANALOGUES

Jones, Martin,Rana, Kishore K.,Ward, John G.,Young, Rodney C.

, p. 5353 - 5356 (2007/10/02)

Short and convenient syntheses of PtdIns 4P and PtdIns analogues based on selective phosphorylation of (+)-2,3:5,6-di-O-isopropylidine-myo-inositol are presented.

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