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6-benzyl-6-azabicyclo[3.2.1]octan-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16607-47-9

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16607-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16607-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,0 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16607-47:
(7*1)+(6*6)+(5*6)+(4*0)+(3*7)+(2*4)+(1*7)=109
109 % 10 = 9
So 16607-47-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H17NO/c16-14-7-12-6-13(8-14)15(10-12)9-11-4-2-1-3-5-11/h1-5,12-13H,6-10H2

16607-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-benzyl-6-azabicyclo[3.2.1]octan-3-one

1.2 Other means of identification

Product number -
Other names 6-Azabicyclo[3.2.1]octan-3-one,6-(phenylmethyl)

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:16607-47-9 SDS

16607-47-9Relevant academic research and scientific papers

PHARMACEUTICAL COMPOSITIONS AND METHODS FOR RELIEVING PAIN AND TREATING CENTRAL NERVOUS SYSTEM DISORDERS

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Page/Page column 68, (2008/06/13)

Patients susceptible to or suffering from disorders, such as central nervous system disorders, which are characterized by an alteration in normal neurotransmitter release, such as dopamine release (e.g., Parkinsonism, Parkinson's Disease, Tourette's Syndrome, attention deficient disorder, or schizophrenia), are treated by administering a compound of Formulas (1 or 2), as described herein. The compounds of Formulas (1 and 2) are also useful for treating pain, and treating drug addiction, nicotine addiction, and/or obesity. The compounds can exist as individual stereoisomers, racemic mixtures, diastereomers and the like.

Synthesis and Stereoselective Reduction of (+/-)-, (+)- and (-)-6-Substituted-6-azabicyclooctan-3-one

Pitner, J. Bruce,Abraham, Philip,Joo, Young J.,Triggle, David J.,Carroll, F. Ivy

, p. 1375 - 1381 (2007/10/02)

Starting with 6-oxabicyclooct-3-en-7-one 6, a three step, general synthetic route to both racemic and optically active 6-substituted 6-azabicyclooctan-3-ones has been developed.Opening of the lactone ring of 6 with amines gave amides which w

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