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Imidazo[4,5,1-jk][1]benzazepin-2(1H)-one, 4,5,6,7-tetrahydro-7-hydroxy-6-[(1-methylethyl)amino]-, hydrochloride (1:1), (6S,7S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1117752-22-3

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1117752-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1117752-22-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,7,7,5 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1117752-22:
(9*1)+(8*1)+(7*1)+(6*7)+(5*7)+(4*5)+(3*2)+(2*2)+(1*2)=133
133 % 10 = 3
So 1117752-22-3 is a valid CAS Registry Number.

1117752-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (6S,7S)-7-Hydroxy-6-(isopropylamino)-4,5,6,7-tetrahydroimidazo[4, 5,1-jk][1]benzazepin-2(1H)-one hydrochloride (1:1)

1.2 Other means of identification

Product number -
Other names roseoside II

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:1117752-22-3 SDS

1117752-22-3Downstream Products

1117752-22-3Relevant academic research and scientific papers

Synthesis and pharmacological characterization of β2- adrenergic agonist enantiomers: Zilpaterol

Kern, Christopher,Meyer, Thorsten,Droux, Serge,Schollmeyer, Dieter,Miculka, Christian

, p. 1773 - 1777 (2009)

The β-adrenergic agonist 1 (zilpaterol) is used as production enhancer in cattle. Binding experiments of separated enantiomers on recombinant human β2-adrenergic and μ-opioid receptors and functional studies showed that the (-)-1 enantiomer acc

Zilpaterol Enantiomer Compositions and Methods of Making and Using Such Compositions

-

Page/Page column 8, (2010/02/17)

This invention is directed generally to zilpaterol enantiomer compositions and, in particular, to compositions comprising the 6R,7R zilpaterol enantiomer. This invention is also directed to processes for making such compositions; methods for using such compositions to, for example, increase the rate of weight gain, improve feed efficiency, and/or increase carcass leanness in livestock, poultry, and/or fish; and uses of such compositions to make medicaments. This invention is further directed to methods for determining the absolute configurations of zilpaterol enantiomers.

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