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4-Cycloocten-1-one, 8-chloro-, (Z)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138619-95-1 Structure
  • Basic information

    1. Product Name: 4-Cycloocten-1-one, 8-chloro-, (Z)- (9CI)
    2. Synonyms: 4-Cycloocten-1-one, 8-chloro-, (Z)- (9CI)
    3. CAS NO:138619-95-1
    4. Molecular Formula: C8H11ClO
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138619-95-1.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: 4-Cycloocten-1-one, 8-chloro-, (Z)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Cycloocten-1-one, 8-chloro-, (Z)- (9CI)(138619-95-1)
    11. EPA Substance Registry System: 4-Cycloocten-1-one, 8-chloro-, (Z)- (9CI)(138619-95-1)
  • 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: 138619-95-1(Hazardous Substances Data)

138619-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138619-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,1 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138619-95:
(8*1)+(7*3)+(6*8)+(5*6)+(4*1)+(3*9)+(2*9)+(1*5)=161
161 % 10 = 1
So 138619-95-1 is a valid CAS Registry Number.

138619-95-1Downstream Products

138619-95-1Relevant articles and documents

Metal-Catalyzed Organic Photoreactions. Chemo- and Regioselectivities in the CuCl2-Induced Photooxidation of Olefins.

Sato, Tadashi,Yonemochi, Shin-ichi

, p. 7375 - 7384 (1994)

Copper(II) chloride induced the chemo and regioselective chlorohydroperoxidation, as well as the site-selective chlorination of olefins, under photooxygenation conditions.

A SIMPLE SYNTHESIS OF 4-CYCLOHEPTENE-1-CARBOXYLIC ACID

Zakharkin, L. I.,Guseva, P. V.

, p. 1055 - 1056 (2007/10/02)

A simple method is proposed for the production of 4-cycloheptene-1-carboxylic acid from 1,5-cyclooctadiene through 2-chloro-5-cycloocten-1-one oxime.

OXYCHLORINATION OF ALKENES BY CHLOROCHROMATE REAGENTS: A FACILE PREPARATION OF α-CHLOROKETONES, AND COMPETITION BY SUBSTITUENT-DIRECTED OXIDATION.

Guerrero, Angel F.,Kim, Ho-jin,Schlecht, Matthew F.

, p. 6707 - 6710 (2007/10/02)

Cyanopyridinium chlorochromate effects a facile preparation of α-chloroketones from simple alkenes, cycloocta-1,5-diene and cyclododeca-1,5,9-triene; 1-methylcaclooct-4-en-1-ol undergoes oxidative cyclization.

Metal-Catalyzed Organic Photoreactions. One-Step Synthesis of Chlorinated Ketones from Olefins by Photooxidation in the Presence of Iron(III) Chloride

Kohda, Akira,Ueda, Keiko,,Sato, Tadashi

, p. 509 - 515 (2007/10/02)

Under photooxidation in pyridine in the presence of FeCl3, mono- and disubstituted olefins gave α-chloro ketones, while tri- and tetrasubstituted olefins gave dichloro ketones with a C-C bond cleavage.The reaction was interpreted in terms of an electron-transfer mechanism occurring within the coordination sphere of the iron ion

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