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35194-31-1

6-Octen-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 35194-31-1 Structure

  • Basic information

    1. Product Name: 6-Octen-2-one
    2. Synonyms: 6-Octen-2-one
    3. CAS NO:35194-31-1
    4. Molecular Formula: C8H14O
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 35194-31-1.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: 6-Octen-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Octen-2-one(35194-31-1)
    11. EPA Substance Registry System: 6-Octen-2-one(35194-31-1)

  • 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: 35194-31-1(Hazardous Substances Data)

35194-31-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35194-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,9 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35194-31:
(7*3)+(6*5)+(5*1)+(4*9)+(3*4)+(2*3)+(1*1)=111
111 % 10 = 1
So 35194-31-1 is a valid CAS Registry Number.

35194-31-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name oct-6-en-2-one

1.2 Other means of identification

Product number -
Other names (E)-Oct-6-en-2-one

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:35194-31-1 SDS

35194-31-1Downstream Products

35194-31-1Relevant articles and documents

A Novel Bicyclic Ketal Fragmentation Reaction

Bjorklund, Michael,Jun, Jong Gab,Mundy, Bradford P.

, p. 3895 - 3898 (2007/10/02)

Bicyclic ketals of the 6,8-dioxabicyclooctane series are specifically cleaved to give δ,ε-unsaturated ketones by treatment of the ketal with acetyl iodide.

APPLICATIONS OF THE TANDEM -WITTIG-OXY-COPE REARRANGEMENT TO SYNTHESIS OF exo-BREVICOMIN AND OXOCRINOL. THE SCOPE AND LIMITATION OF THE SIGMATROPIC SEQUENCES AS A SYNTHETIC METHOD FOR δ,ε-UNSATURATED KETONES

Mikami, Koichi,Nakai, Takeshi

, p. 1349 - 1352 (2007/10/02)

The synthetic utility of the title sigmatropic sequence is illustrated in the syntheses of (E)-6-nonen-2-one, a precursor of exo-brevicomin, and oxocrinol.The scope and limitation of this sequence as a synthetic method for δ,ε-unsaturated ketones are also discussed.

REACTION DES HEXADIENE-1,5 OLS-3 AVEC LE TRIFLUOROACETATE MERCURIQUE; TRANSPOSITION D'OXY-COPE A TEMPERATURE AMBIANTE.

Bluthe, Norbert,Malacria, Max,Gore, Jacques

, p. 4263 - 4266 (2007/10/02)

Tertiary 1,5-hexadien-3-ols 1 are transformed to δ-ethylene ketones 2 in 35-75 percent yield by treatment with one equivalent of mercuric trifluoroacetate and subsequent demercuration using sodium borohydride (Scheme I, Table).

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