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110967-07-2

1-isopropyloctahydroazocin-2,8-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 110967-07-2 Structure

  • Basic information

    1. Product Name: 1-isopropyloctahydroazocin-2,8-dione
    2. Synonyms: 1-isopropyloctahydroazocin-2,8-dione
    3. CAS NO:110967-07-2
    4. Molecular Formula:
    5. Molecular Weight: 183.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 110967-07-2.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: 1-isopropyloctahydroazocin-2,8-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-isopropyloctahydroazocin-2,8-dione(110967-07-2)
    11. EPA Substance Registry System: 1-isopropyloctahydroazocin-2,8-dione(110967-07-2)

  • 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: 110967-07-2(Hazardous Substances Data)

110967-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110967-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,9,6 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 110967-07:
(8*1)+(7*1)+(6*0)+(5*9)+(4*6)+(3*7)+(2*0)+(1*7)=112
112 % 10 = 2
So 110967-07-2 is a valid CAS Registry Number.

110967-07-2Downstream Products

110967-07-2Relevant articles and documents

Ruthenium Tetroxide Oxidation of N-Alkyllactams

Yoshifuji, Shigeyuki,Arakawa, Yukimi,Nitta, Yoshihiro

, p. 357 - 363 (2007/10/02)

Ruthenium tetroxide (RuO4) oxidation of N-alkyllactams proceeded regioselectively depending on the size of lactam ring, except for the seven-membered ring.Four- and eight-membered N-methyl- and N-ethyllactams were oxidized at the exocyclic α-carbon adjacent to nitrogen to produce the N-acyllactams and NH-lactams, while five- and six-membered lactams underwent endocyclic oxidation to yield the cyclic imides.Oxidation of seven-membered lactams yielded a mixture of products arising from both exocyclic and endocyclic oxidations.These regioselectivities were confirmed in the oxidation of substrates having a tertiary carbon at the oxidation position.Keywords---oxidation; ruthenium tetroxide oxidation; regioselective oxidation; hydroxylation; imide synthesis; N-alkyllactam; N-acyllactams; imide; ruthenium tetroxide; two-phase method

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