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(Z)-2-Methyl-4-nonene is an organic compound with the molecular formula C10H20. It is a colorless liquid with a strong, pungent odor. This alkene is characterized by a double bond between the 2nd and 3rd carbon atoms, with a methyl group attached to the 2nd carbon. It is an isomer of 2-methyl-4-nonene, differing in the position of the double bond. (Z)-2-Methyl-4-nonene is used as a fragrance ingredient and a chemical intermediate in the synthesis of various compounds. It is insoluble in water but soluble in organic solvents. Due to its volatile nature, it is often used in the perfume industry and as a solvent in various chemical processes.

51090-05-2

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51090-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51090-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,9 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51090-05:
(7*5)+(6*1)+(5*0)+(4*9)+(3*0)+(2*0)+(1*5)=82
82 % 10 = 2
So 51090-05-2 is a valid CAS Registry Number.

51090-05-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-non-4c-ene

1.2 Other means of identification

Product number -
Other names (Z)-2-Methyl-4-nonen

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:51090-05-2 SDS

51090-05-2Downstream Products

51090-05-2Relevant academic research and scientific papers

THE EFFECT OF CROWN ETHER ON STERIC HINDRANCE TO BASE APPROACH IN BIMOLECULAR ELIMINATION: EVIDENCE AGAINST CLUMP AGGREGATE MODEL OF ION-PAIRED ALKOXIDE BASE

Pankova, Magdalena,Zavada, Jiri

, p. 3150 - 3159 (2007/10/02)

The effect of 18-crown-6-ether upon geometrical orientation and rates was investigated in tert-C4H9OK-tert-C4H9OH promoted anti-elimination from two homologous series of tosylates, RCH2CHOTsC5H11 and RCHOTsCH2C5H11 (R = H, CH3, C2H5, n-C3H5, iso-C3H7, tert-C4H9).Steric requirements of the cis- and trans-stereoselective base species operating in the reaction in the absence and in the presence of the crown ether, respectively, have been assessed.An unambiguous distinction has been made between two pending models of the cis-stereoselective (ion-paired) base.

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