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7-Oxabicyclo[4.1.0]heptane-3-carbonitrile is a chemical compound with the molecular formula C8H9NO. It is a heterocyclic compound, specifically a bicyclic structure with a seven-membered ring and an oxygen atom. The compound features a carbonitrile group (-CN) attached to the third carbon atom, which is part of the oxabicyclo ring system. This molecule is known for its unique structure and potential applications in organic synthesis and pharmaceutical chemistry. It is an important intermediate in the synthesis of various biologically active compounds and can be used in the preparation of complex molecules with potential therapeutic properties.

141-40-2

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141-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141-40-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141-40:
(5*1)+(4*4)+(3*1)+(2*4)+(1*0)=32
32 % 10 = 2
So 141-40-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO/c8-4-5-1-2-6-7(3-5)9-6/h5-7H,1-3H2

141-40-2SDS

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 7-oxabicyclo[4.1.0]heptane-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 7-Oxabicyclo[4.1.0]heptane-3-carbonitrile

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 -
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More Details:141-40-2 SDS

141-40-2Downstream Products

141-40-2Relevant academic research and scientific papers

From aldehydes to nitriles, a general and high yielding transformation using HOF·CH3CN complex

Carmeli, Mira,Shefer, Neta,Rozen, Shlomo

, p. 8969 - 8972 (2007/10/03)

N,N-Dimethylhydrazones of aldehydes undergo a rapid oxidative cleavage to form nitriles in very high yields on reaction with HOF·CH3CN under mild conditions. The reaction is chemoselective and proceeds rapidly without racemization. The nitriles were resistant to further oxidation, even when a large excess of the reagent was employed.

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