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Bicyclo[4.1.0]heptane, 7-(methylethylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53282-47-6

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53282-47-6 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 96, p. 4562, 1974 DOI: 10.1021/ja00821a034

Check Digit Verification of cas no

The CAS Registry Mumber 53282-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,2,8 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53282-47:
(7*5)+(6*3)+(5*2)+(4*8)+(3*2)+(2*4)+(1*7)=116
116 % 10 = 6
So 53282-47-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H16/c1-7(2)10-8-5-3-4-6-9(8)10/h8-9H,3-6H2,1-2H3

53282-47-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-propan-2-ylidenebicyclo[4.1.0]heptane

1.2 Other means of identification

Product number -
Other names Bicyclo[4.1.0]heptane,7-(1-methylethylidene)

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:53282-47-6 SDS

53282-47-6Downstream Products

53282-47-6Relevant academic research and scientific papers

Mild Generation of Alkylidenecarbenes from (Tosylazo)alkenes and Silylvinyl Triflates. Mode of Decomposition and Nature of the Carbene Intermediates

Fox, Dennis P.,Bjork, Jon A.,Stang, Peter J.

, p. 3994 - 4002 (2007/10/02)

(Tosylazo)alkenes, R2C=CHN=NTs, decomposed in olefin-solvent mixtures both under neutral conditions at room temperature and with amine bases present to produce alkylidenecyclopropanes in moderate to good yields.Diazoalkenes, R2C=C=N2, were implicated as t

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