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37025-59-5

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37025-59-5 Usage

General Description

(IR,2S)-I-N,N-Diethylnorephedrine HCL is a chemical compound that belongs to the class of nor-ephedrine derivatives. It is the hydrochloride salt form of the (IR,2S)-I-N,N-Diethylnorephedrine, which is a sympathomimetic amine and a stereoisomer of ephedrine. (IR,2S)-I-N,N-Diethylnorephedrine HCL is commonly used in the pharmaceutical industry as a nasal decongestant and bronchodilator due to its stimulant and vasoconstrictive properties. It works by targeting adrenergic receptors in the respiratory tract, leading to the relaxation of smooth muscles and the reduction of nasal congestion. Additionally, it may also have potential applications in the treatment of obesity and as a stimulant. However, its use is strictly regulated due to its potential for abuse and side effects, such as increased heart rate and elevated blood pressure.

Check Digit Verification of cas no

The CAS Registry Mumber 37025-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,2 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37025-59:
(7*3)+(6*7)+(5*0)+(4*2)+(3*5)+(2*5)+(1*9)=105
105 % 10 = 5
So 37025-59-5 is a valid CAS Registry Number.

37025-59-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(diethylamino)-1-phenylpropan-1-ol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:37025-59-5 SDS

37025-59-5Upstream product

37025-59-5Downstream Products

37025-59-5Relevant articles and documents

THE STEREOSELECTIVE REDUCTION OF α-AMINOPROPIOPHENONE DERIVATIVES WITH SODIUM BOROHYDRIDE

Kametani, Tetsuji,Kigasawa, Kazuo,Hiiragi, Mineharu,Wagatsuma, Nagatoshi,Kohagizawa, Toshitaka,Inoue, Hitoshi

, p. 775 - 778 (2007/10/02)

The ratio of erythro and threo products from the sodium borohydride reduction of the hydrochlorides, and other acid salts, of α-aminopropiophenone derivatives was determined.It was found that this procedure resulted in stereoselective formation of erythro-2-amino-1-phenylpropanols in contrast to sodium borohydride reduction of the corresponding free bases.The method was successfully applied to the synthesis of dl-erythro-2-(4-benzylpiperidino)-1-(4-hydroxyphenyl)propanol which has been used as a vasodilator.

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