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2-chlorocyclohexyl isobutyrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76475-06-4 Structure
  • Basic information

    1. Product Name: 2-chlorocyclohexyl isobutyrate
    2. Synonyms: 2-chlorocyclohexyl isobutyrate
    3. CAS NO:76475-06-4
    4. Molecular Formula:
    5. Molecular Weight: 204.697
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76475-06-4.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: 2-chlorocyclohexyl isobutyrate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-chlorocyclohexyl isobutyrate(76475-06-4)
    11. EPA Substance Registry System: 2-chlorocyclohexyl isobutyrate(76475-06-4)
  • 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: 76475-06-4(Hazardous Substances Data)

76475-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76475-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,7 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76475-06:
(7*7)+(6*6)+(5*4)+(4*7)+(3*5)+(2*0)+(1*6)=154
154 % 10 = 4
So 76475-06-4 is a valid CAS Registry Number.

76475-06-4Downstream Products

76475-06-4Relevant articles and documents

Visible-light-triggered Catalytic Halohydrin Synthesis from Epoxides and Trichloroacetonitrile by Copper and Iron Salts

Toda, Yasunori,Tanaka, Katsumi,Matsuda, Riki,Suga, Hiroyuki

, p. 1469 - 1471 (2019)

Preparation of vicinal halohydrins, in which copper or iron chlorides catalyze the ring-opening reaction of epoxides with visible light effectively, is described. The use of trichloroacetonitrile as a halogen source enables catalytic HCl generation under the mild conditions. This method can also be applied to the aziridine ring-opening reaction.

Reactions du n=chloroparatoluenesulfonamidate de sodium (chloramine t) sur les olefines en miliu acide organique

Damin, Bernard,Garapon, Jacques,Sillion, Bernard

, p. 1709 - 1710 (2007/10/02)

Vic. chloro-acetoxy and vic. chloro-tosylamino alcanes are the main products of the electrophilic reaction of chloramine T on olefins in acetic acid. The stereochemistry of the acetoxy chloration of the 2-butenes and cyclohexene is trans.

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