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9-oxabicyclo[3.3.1]non-2-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40164-27-0

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40164-27-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40164-27-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,6 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40164-27:
(7*4)+(6*0)+(5*1)+(4*6)+(3*4)+(2*2)+(1*7)=80
80 % 10 = 0
So 40164-27-0 is a valid CAS Registry Number.

40164-27-0SDS

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 9-oxabicyclo[3.3.1]non-3-ene

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:40164-27-0 SDS

40164-27-0Downstream Products

40164-27-0Relevant academic research and scientific papers

Heats of Hydrogenation of Some Vinyl Ethers and Related Compounds

Allinger, N. L.,Glaser, John A.,Davis, H. E.,Rogers, Donald W.

, p. 658 - 661 (1981)

The heats of hydrogenation of a number of vinyl ethers and related compounds have been measured in hexane solution.The presence of the oxygen has a small to moderate effect on the magnitudes of these numbers, depending on the situation, and may either stabilize or destabilize the double bonds relative to the hydrogenation products.The results can, in the main, be interpreted in a straightforward way using resonance and induction arguments.

Transformation of hydroxycycloalkanones to oxabicycloalkenes

Kraemer, Guido,Detert, Heiner,Meier, Herbert

scheme or table, p. 2201 - 2208 (2010/04/29)

Oxabicycloalkenes, which represent anti-Bredt enol ethers, can be generated by catalytic dehydration of the hemiacetals of hydroxycycloalkanones (Method I). Another option is provided by the transformation of hydroxycycloalkanones to the corresponding 1,2,3-selenadiazoles and their thermal fragmentation on Cu powder (Method II). The intermediate hydroxycycloalkynes show a transannular addition of the OH group to the triple bond. Altogether seven new oxabicycloalk-1-enes were obtained by this methods.

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