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2415-95-4

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2415-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2415-95-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2415-95:
(6*2)+(5*4)+(4*1)+(3*5)+(2*9)+(1*5)=74
74 % 10 = 4
So 2415-95-4 is a valid CAS Registry Number.

2415-95-4SDS

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 ethyl 2,2,3,3-tetramethylcyclopropanecarboxylate

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:2415-95-4 SDS

2415-95-4Relevant articles and documents

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Wharton,P.S.,Bair,T.I.

, p. 1681 - 1684 (1965)

-

Polymeric dicarbonyl ruthenium(I) acetate - An efficient catalyst for alkene cyclopropanation with diazoacetates

Maas,Werle,Alt,Mayer

, p. 881 - 888 (2007/10/02)

The polymeric complex [Ru2(CO)4(μ-OAc)2](n) is the first Ru(I) catalyst that efficiently catalyzes cyclopropanation of alkenes with diazoacetic esters. The related dinuclear catalyst Ru2(CO)4(μ-OAc)2(MeCN)2 shows a similar performance only for cyclopropanation of monosubstituted alkenes.

Novel process for the preparation of tetra-substituted cyclopropane compounds

-

, (2008/06/13)

A process for the preparation of tetrasubstituted cyclopropane compounds of the formula STR1 wherein Y is selected from the group consisting of --CN and --COOR, R is selected from the group consisting of hydrogen and alkyl of 1 to 6 carbon atoms and R1, R2, R3 and R4 are individually selected from alkyl of 1 to 4 carbon atoms or R1 and R2 or R3 and R4 together with the carbon atoms to which they are attached form a carbon homocycle of 3 to 6 carbon atoms with the 2 substituents not forming the ring being alkyl of 1 to 4 carbon atoms or R1 and R2 on the one hand and R3 and R4 on the other together with the carbon atom to which they are attached form a carbon homocycle of 3 to 6 carbon atoms which are useful intermediates for the preparation of insecticidal esters and novel intermediates.

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