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56888-88-1

2-METHYL-2-UNDECENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 56888-88-1 Structure

  • Basic information

    1. Product Name: 2-METHYL-2-UNDECENE
    2. Synonyms: 2-METHYL-2-UNDECENE
    3. CAS NO:56888-88-1
    4. Molecular Formula: C12H24
    5. Molecular Weight: 168.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 56888-88-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-METHYL-2-UNDECENE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-METHYL-2-UNDECENE(56888-88-1)
    11. EPA Substance Registry System: 2-METHYL-2-UNDECENE(56888-88-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 56888-88-1(Hazardous Substances Data)

56888-88-1 Usage

Synthesis Reference(s)

Tetrahedron Letters, 16, p. 3837, 1975 DOI: 10.1016/S0040-4039(00)91289-9

Check Digit Verification of cas no

The CAS Registry Mumber 56888-88-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,8 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56888-88:
(7*5)+(6*6)+(5*8)+(4*8)+(3*8)+(2*8)+(1*8)=191
191 % 10 = 1
So 56888-88-1 is a valid CAS Registry Number.

56888-88-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylundec-2-ene

1.2 Other means of identification

Product number -
Other names 2-Undecene,2-methyl

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:56888-88-1 SDS

56888-88-1Relevant articles and documents

Fishing for the right catalyst for the cross-metathesis reaction of methyl oleate with 2-methyl-2-butene

Sytniczuk,Kajetanowicz,Grela

, p. 1284 - 1296 (2017/05/05)

The activity of various Ru-alkylidene olefin metathesis catalyst types on the outcome of cross-metathesis of methyl oleate with 2-methyl-2-butene was studied.

Zinc-mediated synthesis of tertiary alkyl selenides from tertiary alkyl halides

Krief, Alain,Derock, Michel,Lacroix, Damien

, p. 2832 - 2834 (2007/10/03)

Diorganyl selenides are efficiently synthesized from tertiary alkyl halides, selenols or selenolates and zinc dibromide as well as from diselenides in the presence of zinc. Georg Thieme Verlag Stuttgart.

Scandium trifluoromethanesulfonate as an extremely active Lewis acid catalyst in acylation of alcohols with acid anhydrides and mixed anhydrides

Ishihara, Kazuaki,Kubota, Manabu,Kurihara, Hideki,Yamamoto, Hisashi

, p. 4560 - 4567 (2007/10/03)

Scandium trifluoromethanesulfonate (triflate), which is commercially available, is a practical and useful Lewis acid catalyst for acylation of alcohols with acid anhydrides or the esterification of alcohols by carboxylic acids in the presence of p-nitrobenzoic anhydrides. The remarkably high catalytic activity of scandium triflate can be used for assisting the acylation by acid anhydrides of not only primary alcohols but also sterically-hindered secondary or tertiary alcohols. The method presented is especially effective for selective macrolactonization of ω-hydroxy carboxylic acids.

Reaction of α-Silyl Esters with Grignard Reagents: A Synthesis of β-Keto Silanes and Ketones. Preparation of the Douglas Fir Tussock Moth Pheromone

Larson, Gerald L.,Hernandez, David,Lopez-Cepero, Ingrid Montes de,Torres, Luz E.

, p. 5260 - 5267 (2007/10/02)

A variety of α-diphenylmethylsilyl esters have been prepared and reacted with Grignard reagents.The reaction is relatively slow in refluxing THF and can be controlled to allow the addition of 1 equiv of the Grignard reagent, providing the corresponding β-keto silane.Protiodesilylation of the β-keto silane results in the overall conversion of an ester to a ketone.This ester to ketone methodology has been applied to a two-step synthesis of the pheromone of the Douglas fir tussock moth.The β-keto silanes are viable precursors to regioselectively generated enol silyl ethers.The reaction of ethyl 2-methyl-2-(diphenylmethylsilyl)propionate with vinylmagnesium bromide or 2-methyl 1-propenylmagnesium bromide results in the addition of 2 equiv of the Grignard reagent, the second in a Michael fashion.

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