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38846-08-1

4,4-dimethyl-3-dimethylamino-1-phenylhex-5-en-1-yne is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 38846-08-1 Structure

  • Basic information

    1. Product Name: 4,4-dimethyl-3-dimethylamino-1-phenylhex-5-en-1-yne
    2. Synonyms: 4,4-dimethyl-3-dimethylamino-1-phenylhex-5-en-1-yne
    3. CAS NO:38846-08-1
    4. Molecular Formula:
    5. Molecular Weight: 227.349
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 38846-08-1.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: 4,4-dimethyl-3-dimethylamino-1-phenylhex-5-en-1-yne(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,4-dimethyl-3-dimethylamino-1-phenylhex-5-en-1-yne(38846-08-1)
    11. EPA Substance Registry System: 4,4-dimethyl-3-dimethylamino-1-phenylhex-5-en-1-yne(38846-08-1)

  • 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: 38846-08-1(Hazardous Substances Data)

38846-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38846-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,4 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38846-08:
(7*3)+(6*8)+(5*8)+(4*4)+(3*6)+(2*0)+(1*8)=151
151 % 10 = 1
So 38846-08-1 is a valid CAS Registry Number.

38846-08-1Relevant articles and documents

Base Catalysed Rearrangements involving Ylide Intermediates. Part 6. The Rearrangements of Diallyl- and Allylpropynyl-ammonium Cations in Protic Media

Laird, Trevor,Ollis, W. David,Sutherland, Ian O.

, p. 1477 - 1486 (2007/10/02)

The base catalysed rearrangements of the cations (1d-j) in aqueous solution yield the isomeric cations (15) or the aldehydes (10) and (11), or mixtures of (15), (10), and (11).This contrasts dramatically with the transformations observed for the cations (1) in aprotic solvents.The cations (15) undergo Hofmann elimination to the naphthalenic amines (12) or (13) and (14).The methiodide of amine (13g) shows a novel consequence of restricted rotation.The n.m.r. spectrum of the methiodide shows that the two protons of the methylene group are diastereotopic.

Base-catalysed rearrangement of allyl-propynyl ammonium cations and a novel synthetic route to substituted biphenyls

Jemison,Laird,Ollis

, p. 556 - 557 (2007/10/06)

Base-catalysed rearrangement of the salts (I) in aprotic media gives the amines (II) and (III); the amines (II) on heating yield the biphenyl derivatives (V).

Base-catalysed rearrangement of allyl-propynyl ammonium cations in protic media

Laird,Ollis

, p. 557 - 559 (2007/10/05)

The base-catalysed rearrangement of the allylpropynyl ammonium cations (I) in aqueous solution yields either the isomeric cations (II) or the aldehydes (III) and (IV), or mixtures of (II), (III), and (IV); this result contrasts dramatically with the trans

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