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2-Azabicyclo[3.3.1]nonan-9-one, 5-(3-methoxyphenyl)-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88550-34-9

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88550-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88550-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,5 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88550-34:
(7*8)+(6*8)+(5*5)+(4*5)+(3*0)+(2*3)+(1*4)=159
159 % 10 = 9
So 88550-34-9 is a valid CAS Registry Number.

88550-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3-methoxyphenyl)-2-methyl-2-azabicyclo[3.3.1]nonan-9-one

1.2 Other means of identification

Product number -
Other names 5-(3-methoxy-phenyl)-2-methyl-2-aza-bicyclo[3.3.1]nonan-9-one

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:88550-34-9 SDS

88550-34-9Relevant academic research and scientific papers

BIASED POTENT OPIOID-LIKE AGONISTS AS IMPROVED MEDICATIONS TO TREAT CHRONIC AND ACUTE PAIN AND METHODS OF USING THE SAME

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Paragraph 00148, (2019/10/15)

The present invention is directed to a compound having Formula (I) and its enantiomer: wherein the definitions of n, R, X, Y and Y3, and Z are provided in the disclosure. The invention is also directed to pharmaceutical compositions of the disc

Probes for narcotic receptor mediated phenomena. 34. Synthesis and structure - Activity relationships of a potent μ-agonist δ-antagonist and an exceedingly potent antinociceptive in the enantiomeric C9-substituted 5-(3-hydroxyphenyl)-N-phenylethylmorphan

Hiebel, Anne-Cécile,Yong, Sok Lee,Bilsky, Edward,Giuvelis, Denise,Deschamps, Jeffrey R.,Parrish, Damon A.,Aceto, Mario D.,May, Everette L.,Harris, Louis S.,Coop, Andrew,Dersch, Christina M.,Partilla, John S.,Rothman, Richard B.,Cheng, Kejun,Jacobson, Arthur E.,Rice, Kenner C.

, p. 3765 - 3776 (2008/03/11)

Both of the enantiomers of 5-(3-hydroxyphenyl)-N-phenylethylmorphan with C9α-methyl, C9-methylene, C9-keto, and C9α- and C9β-hydroxy substituents were synthesized and pharmacologically evaluated. Three of the 10 compounds, (1R,5R,9S)-(-)-9-hydroxy-5-(3-hy

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