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2,2,5-Trimethyl-3-((S)-1-phenyl-ethylamino)-hexanoic acid is a complex organic compound with the molecular formula C19H29NO2. It is a chiral molecule, with the (S)-configuration indicating that it is the levorotatory enantiomer. 2,2,5-Trimethyl-3-((S)-1-phenyl-ethylamino)-hexanoic acid is characterized by the presence of three methyl groups (-CH3) at the 2nd, 2nd, and 5th carbon atoms, respectively, and a phenylethylamino group attached to the 3rd carbon. The phenylethylamino group consists of a phenyl ring (C6H5) and an ethylamine chain (-CH2CH2NH2). The carboxylic acid group (-COOH) is present at the 6th carbon, giving the molecule its acidic properties. 2,2,5-Trimethyl-3-((S)-1-phenyl-ethylamino)-hexanoic acid is known for its potential applications in pharmaceuticals and as a building block for the synthesis of various drugs, particularly those targeting the central nervous system.

76368-07-5

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76368-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76368-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,6 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76368-07:
(7*7)+(6*6)+(5*3)+(4*6)+(3*8)+(2*0)+(1*7)=155
155 % 10 = 5
So 76368-07-5 is a valid CAS Registry Number.

76368-07-5Downstream Products

76368-07-5Relevant academic research and scientific papers

ASYMMETRIC SYNTHESIS OF β-LACTAMS. I. THE REACTION OF DIMETHYLKETENE SILYL ACETAL WITH (S)-ALKYLIDENE(1-ARYLETHYL)AMINES PROMOTED BY TITANIUM TETRACHLORIDE

Ojima, Iwao,Inaba, Shin-ichi

, p. 2077 - 2080 (2007/10/02)

Asymmetric synthesis of β-lactams by means of the reaction of dimethyl-ketene silyl acetal with (S)-alkylidene(1-arylethyl)amines in the presence of titanium tetrachloride was studied.The extent of the asymmetric induction was in the range of 44-78percent (diastereomeric purity 72-89percent) and the (S)-configuration was turned to be preferentially induced at the 4C position of the resulting β-lactams.

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