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CAS

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31274-14-3

6-phenylhexanaMide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 31274-14-3 Structure

  • Basic information

    1. Product Name: 6-phenylhexanaMide
    2. Synonyms: 6-phenylhexanaMide
    3. CAS NO:31274-14-3
    4. Molecular Formula: C12H17NO
    5. Molecular Weight: 191.26948
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 31274-14-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 386.6°C at 760 mmHg
    3. Flash Point: 187.6°C
    4. Appearance: /
    5. Density: 1.011g/cm3
    6. Vapor Pressure: 3.5E-06mmHg at 25°C
    7. Refractive Index: 1.524
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 6-phenylhexanaMide(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-phenylhexanaMide(31274-14-3)
    12. EPA Substance Registry System: 6-phenylhexanaMide(31274-14-3)

  • 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: 31274-14-3(Hazardous Substances Data)

31274-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31274-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,7 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 31274-14:
(7*3)+(6*1)+(5*2)+(4*7)+(3*4)+(2*1)+(1*4)=83
83 % 10 = 3
So 31274-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c13-12(14)10-6-2-5-9-11-7-3-1-4-8-11/h1,3-4,7-8H,2,5-6,9-10H2,(H2,13,14)

31274-14-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-phenylhexanamide

1.2 Other means of identification

Product number -
Other names 6-Phenyl-capronamid

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:31274-14-3 SDS

31274-14-3Relevant articles and documents

Hypervalent iodine catalyzed hofmann rearrangement of carboxamides using oxone as terminal oxidant

Yoshimura, Akira,Middleton, Kyle R.,Luedtke, Matthew W.,Zhu, Chenjie,Zhdankin, Viktor V.

, p. 11399 - 11404 (2013/02/23)

Hofmann rearrangement of carboxamides to carbamates using Oxone as an oxidant can be efficiently catalyzed by iodobenzene. This reaction involves hypervalent iodine species generated in situ from catalytic amount of PhI and Oxone in the presence of 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) in aqueous methanol solutions. Under these conditions, Hofmann rearrangement of various carboxamides affords corresponding carbamates in high yields.

Syntheses and Rearrangements of Spirocyclic Oxaziridines Derived from Unsymmetrical Ketones

Aube, Jeffrey,Hammond, Marlys,Gherardini, Elyse,Takusagawa, Fusao

, p. 499 - 508 (2007/10/02)

Oxaziridines provide useful alternatives to the Beckmann rearrangement and Schmidt reaction for ring enlargement of cyclic ketones.The procedure involves the condensation of the ketone in question with optically active α-methylbenzylamine, oxidation of th

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