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2-Azabicyclo[2.2.1]hept-5-en-3-one, 2-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78805-80-8

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78805-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78805-80-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,0 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78805-80:
(7*7)+(6*8)+(5*8)+(4*0)+(3*5)+(2*8)+(1*0)=168
168 % 10 = 8
So 78805-80-8 is a valid CAS Registry Number.

78805-80-8SDS

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 3-benzyl-3-azabicyclo[2.2.1]hept-5-en-2-one

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:78805-80-8 SDS

78805-80-8Relevant academic research and scientific papers

Rearrangement of 2-Azabicyclohept-5-en-3-ones: Synthesis of cis-3-Aminocyclopentane Carboxylic Acid Derivatives

Palmer, Christopher F.,Parry, Keith P.,Roberts, Stanley M.,Sik, Vladimir

, p. 1021 - 1028 (2007/10/02)

The γ-lactam 4 was converted into the bromo ester 6 and the latter compound was transformed in five steps into the diester 10.Similarly the lactam 4 was converted into the hydroxy amide 17 via the intermediacy of the dihalogeno compound 11.Compounds 10 an

Synthesis of Diphenyl Ether Models of Thyroid Hormones. Diphenyl Ethers Linked to the 3-Oxo-2-azabicycloheptane Ring System as Substrates for Conformational Analysis

Mazzocchi, Paul H.,Ammon, Herman L.,Liu, Leslie,Colicelli, Elena,Ravi, Prasad,Burrows, Elizabeth

, p. 4530 - 4536 (2007/10/02)

A series of diphenyl ethers linked to 2-azabicyclooctan-3-ones and 2-azabicycloheptan-3-ones were synthesized as substrates for conformational analysis using the lanthanide shift reagent NMR technique.The materials were prepared by displacement of the exo-6-tosyloxy bicyclic lactam with the corresponding phenoxide which results in formation of the phenyl ether with retention of stereochemistry.This double-inversion process presumably involves anchimeric assistance by the lactam nitrogen.The synthesis and properties of a number of these systems are described.Complete 13C assignments for the series are presented.

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