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5,5-dimethylcyclohexa-1,3-diene-1,3-diyl di(2,2-dimethylpropanoate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1411539-86-0 Structure
  • Basic information

    1. Product Name: 5,5-dimethylcyclohexa-1,3-diene-1,3-diyl di(2,2-dimethylpropanoate)
    2. Synonyms:
    3. CAS NO:1411539-86-0
    4. Molecular Formula:
    5. Molecular Weight: 308.418
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1411539-86-0.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: 5,5-dimethylcyclohexa-1,3-diene-1,3-diyl di(2,2-dimethylpropanoate)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5,5-dimethylcyclohexa-1,3-diene-1,3-diyl di(2,2-dimethylpropanoate)(1411539-86-0)
    11. EPA Substance Registry System: 5,5-dimethylcyclohexa-1,3-diene-1,3-diyl di(2,2-dimethylpropanoate)(1411539-86-0)
  • 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: 1411539-86-0(Hazardous Substances Data)

1411539-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1411539-86-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,1,5,3 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1411539-86:
(9*1)+(8*4)+(7*1)+(6*1)+(5*5)+(4*3)+(3*9)+(2*8)+(1*6)=140
140 % 10 = 0
So 1411539-86-0 is a valid CAS Registry Number.

1411539-86-0Upstream product

1411539-86-0Downstream Products

1411539-86-0Relevant articles and documents

Acyloxybutadiene tricarbonyl iron complexes as enzyme-triggered CO-releasing molecules (ET-CORMs): A structure-activity relationship study

Romanski, Steffen,Kraus, Birgit,Guttentag, Miguel,Schlundt, Waldemar,Rücker, Hannelore,Adler, Andreas,Neud?rfl, J?rg-Martin,Alberto, Roger,Amslinger, Sabine,Schmalz, Hans-Günther

, p. 13862 - 13875 (2012)

A series of η4-acyloxycyclohexadiene-Fe(CO)3 complexes was prepared and fully characterized by spectroscopic methods including single crystal X-ray diffraction. For this purpose a new synthetic access to differently acylated 1,3- and 1,5-dienol-Fe(CO)3 complexes was developed. The enzymatically triggered CO release from these compounds was monitored (detection of CO through GC and/or by means of a myoglobin assay) and the anti-inflammatory effect of the compounds was assessed by a cellular assay based on the inhibition of NO-production by inducible NO synthase (iNOS). It was demonstrated that the properties (rate of esterase-triggered CO release, iNOS inhibition, cytotoxicity) of the complexes strongly depend on the substitution pattern of the π-ligand and the nature of the acyloxy substituent.

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