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1,1,3,5-pentanetetracarboxylic acid tetramethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 36627-09-5 Structure
  • Basic information

    1. Product Name: 1,1,3,5-pentanetetracarboxylic acid tetramethyl ester
    2. Synonyms: 1,1,3,5-pentanetetracarboxylic acid tetramethyl ester
    3. CAS NO:36627-09-5
    4. Molecular Formula:
    5. Molecular Weight: 304.297
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 36627-09-5.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: 1,1,3,5-pentanetetracarboxylic acid tetramethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1,3,5-pentanetetracarboxylic acid tetramethyl ester(36627-09-5)
    11. EPA Substance Registry System: 1,1,3,5-pentanetetracarboxylic acid tetramethyl ester(36627-09-5)
  • 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: 36627-09-5(Hazardous Substances Data)

36627-09-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36627-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,2 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36627-09:
(7*3)+(6*6)+(5*6)+(4*2)+(3*7)+(2*0)+(1*9)=125
125 % 10 = 5
So 36627-09-5 is a valid CAS Registry Number.

36627-09-5Downstream Products

36627-09-5Relevant articles and documents

A Photoredox Catalysis Approach for the Synthesis of Both the ABDE and the ABCD Cores of Tronocarpine

Becerril-Rodríguez, Enrique,Casta?ón-García, Mario,Contreras-Cruz, David A.,Miranda, Luis D.

, p. 246 - 252 (2020)

A general strategy for the facile construction of both the ABDE and ABCD cores of tronocarpine, chippiine and dippinine alkaloids through the retrosynthetic disconnection of the polycyclic motifs into an indole or tryptamine fragment and a suitably functionalized alkyl chain is presented. The approach is enabled by an efficient Ir(III)-catalyzed, photoredox-mediated radical addition of tetramethyl 1-bromopentane-1,1,3,5-tetracarboxylate and dimethyl 2-bromopentanedioate selectively at C-2 of the indole. Subsequent intramolecular cyclization events furnish the desired ABDE and ABCD polycyclic cores in good preparative yields.

POLYVALENT ESTER COMPOSITION AND MANUFACTURING METHOD THEREFOR

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Paragraph 0035, (2017/06/02)

PROBLEM TO BE SOLVED: To provide a composition having high compatibility with an acryl resin, capable of improving bending property when used for an acryl resin film, excellent in handleability, less in breed out, having nonvolatility or low volatility, environmentally friendly and capable of being used as a plasticizer. SOLUTION: There is provided a polyvalent ester composition containing a compound represented by the formula (1) and having percentage of a compound where total of x and y is 3 of 30 to 99 mol% based on 100 mol% of the compound represented by the formula (1), the polyvalent ester compound and a manufacturing method therefor including a process of reacting acrylic acid ester, an active methylene compound and methylene glutaric acid diester. In general formula (1), A is each independently CN, COCH3 or COOX, B is COOX, X is each independently H, a C1 to 20 substituted or unsubstituted alkyl group and x and y are each independently the number of 0 to 10. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

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