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dimethyl (3-methoxyphenyl)-propanedioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133033-13-3 Structure
  • Basic information

    1. Product Name: dimethyl (3-methoxyphenyl)-propanedioate
    2. Synonyms: dimethyl (3-methoxyphenyl)-propanedioate
    3. CAS NO:133033-13-3
    4. Molecular Formula:
    5. Molecular Weight: 238.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133033-13-3.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: dimethyl (3-methoxyphenyl)-propanedioate(CAS DataBase Reference)
    10. NIST Chemistry Reference: dimethyl (3-methoxyphenyl)-propanedioate(133033-13-3)
    11. EPA Substance Registry System: dimethyl (3-methoxyphenyl)-propanedioate(133033-13-3)
  • 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: 133033-13-3(Hazardous Substances Data)

133033-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133033-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,3 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133033-13:
(8*1)+(7*3)+(6*3)+(5*0)+(4*3)+(3*3)+(2*1)+(1*3)=73
73 % 10 = 3
So 133033-13-3 is a valid CAS Registry Number.

133033-13-3Downstream Products

133033-13-3Relevant articles and documents

Transition metal complexes in organic synthesis. Part 46: Synthesis of 5-arylmethyl-substituted tricarbonyl(1-4-η-cyclohexa-1,3-diene)iron complexes

Knoelker, Hans-Joachim,Graf, Michael,Mangei, Ulrike

experimental part, p. 530 - 535 (2011/10/12)

The reaction of tricarbonyl(η5-cyclohexadienylium) iron tetrafluoroborate 3 with the methyl arylacetate 6, the dimethyl arylmalonate 12, and the di-tert-butyl arylmalonate 14 provides regio- and stereoselectively the tricarbonyliron-complexed 5

1,2-dioxetane derivatives, intermediates for syntheses thereof and methods of producing the intermediates

-

, (2008/06/13)

A chemiluminescent 1,2-dioxetane derivative having a formula (I): STR1 wherein R1 and R4 each represent, individually, hydrogen, an alkyl group, an alkoxyl group, a hydroxyl group, or --OSi(R9 R10 R11) in which R9, R10 and R11 each represent an alkyl group; R2, R3, R5 and R6 each represent, individually, hydrogen or an alkyl group, provided that R2, R3, R5 and R6 each cannot be hydrogen at the same time, and that R2 and R3, and R5 and R6, each taken together, can form a cycloalkyl group; R7 represents an alkyl group; R8 represents hydrogen, an alkoxyl group, a phosphate salt group, or --OSi(R9 R10 R11); intermediates for synthesizing the above 1,2-dioxetane derivative; and methods of producing the intermediates are provided.

Benzothiazepines

-

, (2008/06/13)

A compound selected from the group consisting of all possible isomeric forms, racemic or optically active of a compound of the formula STR1 wherein the substituents are defined in the specification, and their non-toxic, pharmaceutically acceptable acid addition salts having antiarhythmic activity.

DIMETHYL ARYLMALONATES FROM CERIUM(IV) AMMONIUM NITRATE PROMOTED REACTIONS OF DIMETHYL MALONATE WITH AROMATIC COMPOUNDS IN METHANOL

Baciocchi, Enrico,Dell'Aira, Donatella,Ruzziconi, Renzo

, p. 2763 - 2766 (2007/10/02)

Aromatic compounds undergo homolytic malonylation by reaction with cerium(IV) ammonium nitrate and dimethyl malonate in methanol at room temperature.

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