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D-m-Octopamine, also known as 2-(4-hydroxyphenyl)-N,N-dimethylethanamine, is a naturally occurring trace amine and a monoamine neurotransmitter found in various organisms, including insects and crustaceans. It plays a crucial role in the regulation of various physiological processes, such as locomotion, aggression, and stress response. Structurally, it is an isomer of octopamine, differing only in the chirality of the alpha carbon. D-m-Octopamine has been studied for its potential applications in the development of insecticides and other pest control strategies, as it can modulate the nervous system of insects and disrupt their behavior.

5596-07-6

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5596-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5596-07-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,9 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5596-07:
(6*5)+(5*5)+(4*9)+(3*6)+(2*0)+(1*7)=116
116 % 10 = 6
So 5596-07-6 is a valid CAS Registry Number.

5596-07-6SDS

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 (+)-Norphenylephrine

1.2 Other means of identification

Product number -
Other names norphenylephrine

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:5596-07-6 SDS

5596-07-6Downstream Products

5596-07-6Relevant academic research and scientific papers

Asymmetric hydrogenation of α-chloro aromatic ketones catalyzed by η6-arene/TsDPEN-ruthenium(II) complexes

Ohkuma, Takeshi,Tsutsumi, Kunihiko,Utsumi, Noriyuki,Arai, Noriyoshi,Noyori, Ryoji,Murata, Kunihiko

, p. 255 - 257 (2007/10/03)

(Chemical Equation Presented) Asymmetric hydrogenation of various α-chloro aromatic ketones with Ru(OTf)(TsDPEN)(η6-arene) (TsDPEN = N-(p-toluenesulfonyl)-1,2-diphenylethylenediamine) produces the chiral chlorohydrins in up to 98% ee. This reac

A new copper (I)-tetrahydrosalen-catab zed asymmetric henry reaction and its extension to the synthesis of (S)-norphenylephrine

Xiong, Yan,Wang, Fei,Huang, Xiao,Wen, Yuehong,Feng, Xiaoming

, p. 829 - 833 (2007/10/03)

A new chiral hydrogenated salen catalyst has been developed for the asymmetric Henry reaction which produces the expected products in moderate to high yields (up to 98%) with excellent enantioselectivities (up to 96% ee). A variety of aromatic, heteroarom

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