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(2S,6S,10R,14R)-16-[(S)-2-Benzyloxy-1-((3R,7R,11S,15S)-3,7,11,15-tetramethyl-16-oxo-hexadecyloxymethyl)-ethoxy]-2,6,10,14-tetramethyl-hexadecanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

156593-03-2

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156593-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156593-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,5,9 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 156593-03:
(8*1)+(7*5)+(6*6)+(5*5)+(4*9)+(3*3)+(2*0)+(1*3)=152
152 % 10 = 2
So 156593-03-2 is a valid CAS Registry Number.

156593-03-2Relevant academic research and scientific papers

Asymmetric synthesis of cyclo-archaeol and β-glucosyl cyclo-archaeol

Ferrer, Catalina,Fodran, Peter,Barroso, Santiago,Gibson, Robert,Hopmans, Ellen C.,Damste, Jaap Sinninghe,Schouten, Stefan,Minnaard, Adriaan J.

, p. 2482 - 2492 (2013/06/05)

An efficient asymmetric synthesis of cyclo-archaeol and β-glucosyl cyclo-archaeol is presented employing catalytic asymmetric conjugate addition and catalytic epoxide ring opening as the key steps. Their occurrence in deep sea hydrothermal vents has been

Total synthesis of archaeal 36-membered macrocyclic diether lipid

Eguchi, Tadashi,Arakawa, Kenji,Terachi, Takumi,Kakinuma, Katsumi

, p. 1924 - 1933 (2007/10/03)

Total synthesis of archaeal 36-membered macrocyclic diether lipid 2 is reported. The synthesis is based upon stereoselective preparation of functionalized isoprenoid chains, ether-linkage formation between the isoprenoid chains with a glycerol derivative,

The First Synthesis of an Archaebacterial 36-Membered Macrocyclic Diether Lipid

Eguchi, Tadashi,Terachi, Takumi,Kakinuma, Katsumi

, p. 137 - 138 (2007/10/02)

The archaebacterial macrocyclic diether lipid featuring of 36-membered ring is synthesized by the McMurry coupling as a key step.

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