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118577-36-9

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118577-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118577-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,5,7 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 118577-36:
(8*1)+(7*1)+(6*8)+(5*5)+(4*7)+(3*7)+(2*3)+(1*6)=149
149 % 10 = 9
So 118577-36-9 is a valid CAS Registry Number.

118577-36-9SDS

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 ethyl 5-bromo-2-oxocyclohexanecarboxylate

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:118577-36-9 SDS

118577-36-9Relevant articles and documents

Reactivity Patterns in the Rhodium Carbenoid Induced Tandem Cyclization-Cycloaddition Reaction

Padwa, Albert,Hornbuckle, Susan F.,Fryxell, Glen E.,Stull, Paul D.

, p. 817 - 824 (2007/10/02)

The rhodium(II) acetate catalyzed behavior of ο--α-diazoacetophenone was studied.The results obtained are consistent with a mechanism in which the key step involves intramolecular cyclization of the ketocarbenoid onto the oxygen atom of the side chain to give an oxonium ylide intermediate which undergoes either C-H insertion or a competitive 2,3-sigmatropic rearrangement.The reaction of 1-diazo-9-decene-2,5-dione with rhodium(II) acetate results in cyclization of the intermediate rhodium carbenoid to give a six-ring carbonyl ylide which readily undergoes intramolecular dipolar cycloaddition.This reaction does not occur when the keto group of the diazo compound has been replaced by an ester functionality.Similar results were also obtained with cis-2-benzoyl-1-(diazoacetyl)cyclopentane.

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