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α-((1,1-dimethylethyl)amino)methyl)-α-methylbenzenemethanol is a complex organic compound with the molecular formula C13H21NO. It is a derivative of benzyl alcohol, featuring a methyl group (-CH3) attached to the benzene ring and an aminomethyl group (-CH2NH-) connected to the carbon atom adjacent to the hydroxyl group (-OH). The aminomethyl group is further substituted with a tert-butyl group (1,1-dimethylethyl), which consists of two methyl groups attached to a central carbon atom. α-<((1,1-dimethylethyl)amino)methyl>-α-methylbenzenemethanol is known for its potential applications in pharmaceuticals and as a chemical intermediate in the synthesis of various organic compounds. Its unique structure contributes to its reactivity and stability, making it a valuable component in the development of new drugs and chemical products.

55915-75-8

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55915-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55915-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,9,1 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55915-75:
(7*5)+(6*5)+(5*9)+(4*1)+(3*5)+(2*7)+(1*5)=148
148 % 10 = 8
So 55915-75-8 is a valid CAS Registry Number.

55915-75-8Downstream Products

55915-75-8Relevant academic research and scientific papers

Bismuth (III) salts as catalysts in the opening of epoxides by amines

Oussaid, Adyl,Garrigues, Bernard,Oussaid, Boualem,Benyaquad, Fatima

, p. 2315 - 2320 (2002)

BiCl3 and Bi (OTf)3 catalyze the opening of epoxides (1-7) by amines (8-12). High regioselectivities are observed. BiCl3 et Bi (OTf)3 catalysent la reaction d'ouverture des epoxydes (1-7) par les amines (8-12). La reaction est fortement regioselective.

Metal salts as new catalysts for mild and efficient aminolysis of oxiranes

Chini,Crotti,Macchia

, p. 4661 - 4664 (2007/10/02)

A new, simple, efficient, inexpensive, anti stereoselective, highly regioselective method for aminolysis of 1,2-epoxides, by means of metal salts, is described.

Preparation of Vicinal N-Alkylamino Alcohols via Acylation-Rearrangement of Nitrones Followed by Hydride Reduction

Coates, Robert M.,Cummins, Clark H.

, p. 1383 - 1389 (2007/10/02)

Acylation-rearrangement of N-tert-butyl and N-cyclohexyl nitrones of cyclohexanecarboxaldehyde (1), n-butyraldehyde, isobutyraldehyde, 3-cyclohexenecarboxaldehyde, and α-methylpropionaldehyde gave α-pivaloyloxy imines, which underwent reduction with lithi

A CONVENIENT PREPARATION OF β-AMINO ALCOHOLS FROM EPOXIDES AND HALOMAGNESIUM ALKYLAMIDES

Carre, M. C.,Houmounou, J. P.,Caubere, P.

, p. 3107 - 3110 (2007/10/02)

Treatment of epoxides with halomagnesium alkylamides in THF affords the corresponding β-amino alcohols in good yields.

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