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4720-83-6

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4720-83-6 Usage

Uses

6-Oxabicyclo[3.2.1]oct-3-en-7-one is used in the convergent total synthesis of Leustroducsin B.

Check Digit Verification of cas no

The CAS Registry Mumber 4720-83-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,2 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4720-83:
(6*4)+(5*7)+(4*2)+(3*0)+(2*8)+(1*3)=86
86 % 10 = 6
So 4720-83-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O2/c8-7-5-2-1-3-6(4-5)9-7/h1,3,5-6H,2,4H2

4720-83-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-OXABICYCLO[3.2.1]OCT-3-EN-7-ONE

1.2 Other means of identification

Product number -
Other names 1H-Phenalen-1-one,9-ethoxy

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:4720-83-6 SDS

4720-83-6Relevant articles and documents

Nicolaou,Lysenko

, p. 293 (1977)

Catalytic Aza-Wacker Annulation: Tuning Mechanism by the Activation Mode of Amide and Enantioselective Syntheses of Melinonine-E and Strychnoxanthine

Xie, Changmin,Luo, Jisheng,Zhang, Yuping,Huang, Sha-Hua,Zhu, Lili,Hong, Ran

, p. 2386 - 2390 (2018/04/30)

An unprecedented N-substituent of the amide was found to be crucial for the successful annulation to establish 2-azabicyclo[3.3.1]nonane and other ring skeletons in good yield. The novel catalytic aza-Wacker annulation methodology was further illustrated

NOVEL COMPOUNDS

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Page/Page column 23, (2015/02/02)

Novel rapamycin analogues and methods for their production with FKBP and/or MIP inhibitory activity with reduced mTOR inhibitory activity with therapeutic potential e.g. as bacterial virulence inhibitors.

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