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35106-87-7

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35106-87-7 Usage

General Description

1-(2-Methylphenyl)ethanamine Hydrochloride, also known as ephedrine hydrochloride, is a chemical compound that belongs to the class of organic compounds known as phenylpropanolamines. It is an amine derivative that is commonly used as a nasal decongestant, bronchodilator, and stimulant. 1-(2-Methylphenyl)ethanamine Hydrochloride acts as a sympathomimetic agent, meaning it mimics the effects of the sympathetic nervous system by stimulating adrenergic receptors. It is frequently used in over-the-counter medicines for the treatment of asthma, bronchitis, and other respiratory conditions. However, it also has potential for abuse due to its stimulating effects, and is regulated as a controlled substance in some countries.

Check Digit Verification of cas no

The CAS Registry Mumber 35106-87-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,0 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35106-87:
(7*3)+(6*5)+(5*1)+(4*0)+(3*6)+(2*8)+(1*7)=97
97 % 10 = 7
So 35106-87-7 is a valid CAS Registry Number.

35106-87-7Upstream product

35106-87-7Relevant articles and documents

Sequential reductive amination-hydrogenolysis: A one-pot synthesis of challenging chiral primary amines

Nugent, Thomas C.,Negru, Daniela E.,El-Shazly, Mohamed,Hu, Dan,Sadiq, Abdul,Bibi, Ahtaram,Umar, M. Naveed

supporting information; experimental part, p. 2085 - 2092 (2011/10/19)

Difficult-to-access chiral primary amines were formed in good to high yield and ee using a rare example of a one-pot synthesis from prochiral ketones (sequential reductive amination-hydrogenloysis). As a highlight we also demonstrate a one-pot reductive amination-hydrogenolysis-reductive amination (five reactions) of ortho-methoxyacetophenone resulting in the chiral diamine 1-(2-methoxyphenyl)ethyl-(2-pyridylmethyl)-amine (4) (58% overall yield, >99% ee), a new organocatalyst for aqueous enantioselective aldol reactions. Copyright

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