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(+)-2-amino-1-(4-hydroxyphenyl)ethanol (1S)-(+)camphor-10-sulphonate, also known as (+)-norepinephrine bitartrate, is a chemical compound that serves as a pharmaceutical agent. It is a synthetic version of the naturally occurring neurotransmitter norepinephrine, which plays a crucial role in the regulation of various physiological functions, including attention, alertness, and stress response. (+)-2-amino-1-(4-hydroxyphenyl)ethanol (1S)-(+)camphor-10-sulphonate is used in the treatment of conditions such as attention deficit hyperactivity disorder (ADHD) and narcolepsy, where it helps to increase focus and reduce impulsivity. The chemical structure consists of a phenyl ring attached to an aminoethanol group, with a hydroxyl group on the phenyl ring and a camphor-10-sulphonate group providing the tartrate salt form. (+)-2-amino-1-(4-hydroxyphenyl)ethanol (1S)-(+)camphor-10-sulphonate is an essential component in the management of certain neurological and psychiatric disorders, highlighting its significance in modern medicine.

1693-64-7

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1693-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1693-64-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,9 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1693-64:
(6*1)+(5*6)+(4*9)+(3*3)+(2*6)+(1*4)=97
97 % 10 = 7
So 1693-64-7 is a valid CAS Registry Number.

1693-64-7Downstream Products

1693-64-7Relevant academic research and scientific papers

The Resolution and Absolute Configuration by X-Ray Crystallography of the Isomeric Octopamines and Synephrines

Midgley, John M.,Thonoor, Mohan C.,Drake, Alex F.,Williams, Clyde M.,Koziol, Anna E.,Palenik, Gus J.

, p. 963 - 970 (2007/10/02)

Racemates of the naturally occuring biogenic amines, o-, m-, and p-octopamine and p-synephrine, have been resolved by the preparation of suitable diastereomeric salts with antipodes of appropriate organic acids.The circular dichroism (c.d.) curves of (-)-m-octopamine hydrochloride and (-)-m-synephrine hydrochloride were superimposable and of opposite sign to those of the corresponding (-)-p-derivatives.X-ray crystallography of the (-)-3-bromocamphor-8-sulphonate salt of (-)-p-synephrine confirmed (for the first time by direct means in this series of compounds) that the absolute configuration of (-)-p-synephrine is R.It is concluded from the c.d. data that the absolute configuration of (-)-p-octopamine is also R.

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