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101906-25-6

Benzene, [[(2-methyl-4-pentynyl)oxy]methyl]-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101906-25-6 Structure

  • Basic information

    1. Product Name: Benzene, [[(2-methyl-4-pentynyl)oxy]methyl]-, (R)-
    2. Synonyms:
    3. CAS NO:101906-25-6
    4. Molecular Formula: C13H16O
    5. Molecular Weight: 188.269
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101906-25-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzene, [[(2-methyl-4-pentynyl)oxy]methyl]-, (R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, [[(2-methyl-4-pentynyl)oxy]methyl]-, (R)-(101906-25-6)
    11. EPA Substance Registry System: Benzene, [[(2-methyl-4-pentynyl)oxy]methyl]-, (R)-(101906-25-6)

  • 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: 101906-25-6(Hazardous Substances Data)

101906-25-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101906-25-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,9,0 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 101906-25:
(8*1)+(7*0)+(6*1)+(5*9)+(4*0)+(3*6)+(2*2)+(1*5)=86
86 % 10 = 6
So 101906-25-6 is a valid CAS Registry Number.

101906-25-6SDS

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 (2R)-benzyl-(2-methylpent-4-ynyl) ether

1.2 Other means of identification

Product number -
Other names (4R)-5-benzyloxy-4-methylpent-1-yne

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:101906-25-6 SDS

101906-25-6Relevant articles and documents

Total synthesis of (-)-xyloketal D and its enantiomer - Confirmation of absolute stereochemistry

Pettigrew, Jeremy D.,Freeman, Rebecca P.,Wilson, Peter D.

, p. 1640 - 1648 (2004)

The total synthesis of (-)-xyloketal D and its enantiomer have been achieved by the reaction of an orthoquinone methide with (4R)- and (4S)-4,5-dihydro-2,4-dimethylfuran via a diastereoselective inverse electron demand Diels-Alder reaction. This total syn

Toward the synthesis of tulearin C: Stereoselective synthesis of the C1-C18 macrolactone core

Yadav,Venkatesh,Swapnil,Prasad

, p. 2336 - 2339 (2013/06/27)

The asymmetric and convergent synthesis of fully functionalized macrocyclic core of tulearin C is described. Sharpless asymmetric epoxidation, Gillman's reaction, olefin cross metathesis, α aminoxylation, and ring closing metathesis reactions are the key

Synthesis of the C21-C28 segment of pectenotoxin-4

Kolakowski, Robert V.,Williams, Lawrence J.

, p. 4761 - 4764 (2008/02/07)

The synthesis of the C21-C28 segment of pectenotoxin-4 as the C21 Weinreb amide is described. Feasibility studies for the union of a related Weinreb amide and a functionalized alkyne are also reported.

A NEW APPROACH TO 1,7-DIOXASPIROUNDEC-4-ENES VIA METALLATED ALLENOL ETHERS. SYNTHESIS OF LACRIMIN A.

Takle, Andrew,Kocienski, Philip

, p. 4503 - 4516 (2007/10/02)

Key steps in the first total synthesis of Lacrimin A (2) include (a) the use of methoxyallene as an enone-1,3-dianion equivalent; (b) the use of a new copper-catalysed migratory insertion reaction to construct a tri-substituted alkene stereoselectively; and (c) the use of a Pd(0)-catalysed coupling reaction to generate an isochromanone ring.

The 3,4-Dihydro-2H-pyran Approach to (+)-Milbemycin β3. Part 2. An Improved Synthesis of (2R,4S,6S,8R,9S)-2--8,9-dimethyl-4-(dimethyl-t-butylsilyloxy)-1,7-dioxaspiroundecane

Kocienski, Philip J.,Street, Stephen D. A.,Yeates, Clive,Campbell, Simon F.

, p. 2189 - 2194 (2007/10/02)

A more efficient synthesis of the title compound (2), previously used in a total synthesis of (+)-milbemycin β3 (1), is described.The key step in the sequence involves a nucleophilic cleavage of the oxirane (4) by the organocuprate derived from

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