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4545-84-0

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4545-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4545-84-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,4 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4545-84:
(6*4)+(5*5)+(4*4)+(3*5)+(2*8)+(1*4)=100
100 % 10 = 0
So 4545-84-0 is a valid CAS Registry Number.

4545-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names endo,endo-2,6-diacetoxy-cis-bicyclo<3.3.0>octane

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:4545-84-0 SDS

4545-84-0Relevant articles and documents

-

McNeely et al.

, p. 714,723 (1955)

-

Deuterium Kinetic Isotope Effects in the 1,4-Dimethylenecyclohexane Boat Cope Rearrangement

Gajewski, Joseph J.,Jimenez, Jose Leonardo

, p. 468 - 474 (2007/10/02)

In order to examine the extent of bond making in the boat-like 3,3-sigmatropic shift transition states, trans-2,3-dimethyl-1,4-dimethylenecyclohexane (T) and its exomethylene tetradeuteria derivative (TXD) were prepared.The 3,3-shift of TXD at 305 deg C r

Additions of Group 6A and 7A Electrophilic Reagents to Dimethyl endo,endo-Bicyclooct-5-ene-2,3-dicarboxylate: Competitive Formation of γ- and δ-Lactones

Garratt, Dennis G.,Ryan, M. Dominic,Beaulieu, Pierre L.

, p. 839 - 845 (2007/10/02)

The reaction of dimethyl endo,endo-bicyclooct-5-ene-2,3-dicarboxylate with chlorine, bromine, iodine, benzeneselenenyl chloride, and benzenesulphenyl chloride has been studied.Under conditions of kinetic control both γ- and δ-lactones are formed, the δ lactone being predominant except in the case of bromine.The thermodynamic product distributions favored the δ-lactone exclusively.A general mechanistic scheme is proposed.

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