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(S)-N-(1-benzyl-2-hydroxyethyl)hexadecanamide is a complex organic compound with the molecular formula C25H43NO2. It is a chiral molecule, with the "S" indicating that it has the (S)-configuration, meaning the hydroxyl group is on the left side when looking at the molecule from the direction of the carbon chain. The compound consists of a hexadecanamide backbone, which is a long-chain fatty acid amide, and a 1-benzyl-2-hydroxyethyl group attached to the nitrogen atom. The benzyl group provides a phenyl ring, while the 2-hydroxyethyl group adds a hydroxyl group and an ethyl chain. (S)-N-(1-benzyl-2-hydroxyethyl)hexadecanamide is known for its potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of certain drugs and as a building block for more complex molecules. Its unique structure and properties make it a subject of interest for researchers in organic chemistry and drug development.

60847-18-9

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60847-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60847-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,4 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60847-18:
(7*6)+(6*0)+(5*8)+(4*4)+(3*7)+(2*1)+(1*8)=129
129 % 10 = 9
So 60847-18-9 is a valid CAS Registry Number.

60847-18-9Downstream Products

60847-18-9Relevant academic research and scientific papers

Model studies toward scyphostatin: Synthesis of (S)-4-benzyl-3-(p-toluenesulfonyl)-2-oxazolidinone and its effective transformation to (S)-N-(1-benzyl-2-hydroxyethyl)hexadecanamide

Izuhara, Takashi,Yokota, Wakako,Inoue, Munenori,Katoh, Tadashi

, p. 553 - 560 (2007/10/03)

(S)-4-Benzyl-3-(p-toluenesulfonyl)-2-oxazolidinone (6) was synthesized as a simplified model substrate for the cyclohexenone subunit (2) of scyphostatin (1) starting from L-phenylalanine (3). Transformation of 6 to (S)-N-(1-benzyl-2-hydroxyethyl)hexadecan

A NEW DETERMINATION OF THE ABSOLUTE CONFIGURATION OF THE CHIRAL AMINE

Nagao, Yoshimitsu,Yagi, Masahiro,Ikeda, Takao,Fujita, Eiichi

, p. 205 - 208 (2007/10/02)

A new method for assignment of the absolute configuration of the asymmetric carbon atom attached to an amino or imino group using rac.-3-hexadecanoyl-4-methoxycarbonyl-1,3-thiazolidine-2-thione (rac.-HDMTT) (4) is described.

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