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13-Heptadecyn-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56554-77-9

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56554-77-9 Usage

Physical state

Colorless liquid

Melting point

45-47°C

Boiling point

278-282°C

Usage

Flavoring agent and fragrance ingredient in cosmetic and personal care products

Application

Synthetic intermediate in organic chemical synthesis

Potential use

Pharmaceutical industry for the synthesis of biologically active compounds

Chemical properties

Long carbon chain and terminal alkyne group

Value

Valuable building block for the production of various compounds

Check Digit Verification of cas no

The CAS Registry Mumber 56554-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,5 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56554-77:
(7*5)+(6*6)+(5*5)+(4*5)+(3*4)+(2*7)+(1*7)=149
149 % 10 = 9
So 56554-77-9 is a valid CAS Registry Number.

56554-77-9Downstream Products

56554-77-9Relevant academic research and scientific papers

Properties of unusual phospholipids IV: Chemoenzymatic synthesis of phospholipids bearing acetylenic fatty acids

Pisch, Sandra,Bornscheuer, Uwe T.,Meyer, Hartmut H.,Schmid, Rolf D.

, p. 14627 - 14634 (2007/10/03)

14-Octadecynoic (1) and 4-octadecynoic (2) acid were synthesized in high yields (56% and 57%) and incorporated into glycerophosphatidylcholine at sn1- and sn2-position. The head group of these phosphatidylcholines was exchanged using phospholipase D (PLD) in a biphasic system. PLD from Streptomyces antibioticus, Streptomyces sp., peanut and cabbage were studied in this transphosphatidylation reaction. Under optimized conditions (40°C, organic solvent:buffer ratio 1:1.5 (v/v), pH 5.6), the conversion of phosphatidylcholine to the corresponding phospholipids with the head groups glycerol, ethanolamine and L-serine reached 99% at 40°C in 1 h. The quantitative analysis of the transphosphatidylation reactions was performed by TLC-FID.

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