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127727-92-8

trans-3-hexenenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127727-92-8 Structure

  • Basic information

    1. Product Name: trans-3-hexenenitrile
    2. Synonyms: trans-3-hexenenitrile
    3. CAS NO:127727-92-8
    4. Molecular Formula:
    5. Molecular Weight: 95.1442
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127727-92-8.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: trans-3-hexenenitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-3-hexenenitrile(127727-92-8)
    11. EPA Substance Registry System: trans-3-hexenenitrile(127727-92-8)

  • 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: 127727-92-8(Hazardous Substances Data)

127727-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127727-92-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,2 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 127727-92:
(8*1)+(7*2)+(6*7)+(5*7)+(4*2)+(3*7)+(2*9)+(1*2)=148
148 % 10 = 8
So 127727-92-8 is a valid CAS Registry Number.

127727-92-8Relevant articles and documents

TRANS-NITRILATION IN THE SERIES OF 2-ALKENOIC ACIDS

Polivin, Yu. N.,Karakhanov, R. A.,Vinokurov, V. A.,Mikaya, A. I.,Silin, M. A.,Makarshin, S. V.

, p. 1795 - 1798 (2007/10/02)

In the case of the reaction of trans-2-hexenoic acid with acetonitrile it was established that acids of the olefinic series enter into trans-nitrilation with aliphatic nitriles; the reaction is complicated by thermal isomerization both of the initial acid and of the reaction products, i.e., the corresponding nitrile and N-acylamide.Under the conditions of the reaction of trans-2-hexenoic acid with deuteroacetonitrile-d3 1,3-hydride-deuteride shifts occur in the intermediate compounds (the N-acylamides).This leads to a redistribution of the deuterium atoms between the products of the investigated reaction.

Homogeneous Metathesis of Unsaturated Nitriles

Bosma, Ruud H. A.,Kouwenhoven, Arjan P.,Mol, Johannes C.

, p. 1081 - 1082 (2007/10/02)

Unsaturated nitriles of general formula CH2=CHnCN, where 1 = n = 4, undergo metathesis in the presence of the catalyst system tungsten hexachloride-tetramethyltin with maximum reactivity for n = 2.

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