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CAS

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945736-71-0

(E)-1-(3-(3,4-dichlorophenyl)allyl)indoline-2,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 945736-71-0 Structure

  • Basic information

    1. Product Name: (E)-1-(3-(3,4-dichlorophenyl)allyl)indoline-2,3-dione
    2. Synonyms: (E)-1-(3-(3,4-dichlorophenyl)allyl)indoline-2,3-dione
    3. CAS NO:945736-71-0
    4. Molecular Formula:
    5. Molecular Weight: 332.186
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 945736-71-0.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: (E)-1-(3-(3,4-dichlorophenyl)allyl)indoline-2,3-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-1-(3-(3,4-dichlorophenyl)allyl)indoline-2,3-dione(945736-71-0)
    11. EPA Substance Registry System: (E)-1-(3-(3,4-dichlorophenyl)allyl)indoline-2,3-dione(945736-71-0)

  • 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: 945736-71-0(Hazardous Substances Data)

945736-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 945736-71-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,7,3 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 945736-71:
(8*9)+(7*4)+(6*5)+(5*7)+(4*3)+(3*6)+(2*7)+(1*1)=210
210 % 10 = 0
So 945736-71-0 is a valid CAS Registry Number.

945736-71-0Relevant articles and documents

Organocatalytic asymmetric cyanation of isatin derived N-Boc ketoimines

Liu, Yun-Lin,Zhou, Jian

supporting information, p. 4421 - 4423 (2013/06/05)

We report the first catalytic asymmetric cyanation of N-Boc ketoimines, which enables highly enantioselective synthesis of oxindole based α-amino nitriles. An unprecedented tandem aza-Wittig/Strecker reaction is also developed, emerging as a promising strategy for the catalytic asymmetric cyanation of ketoimines formed in situ from achiral ketones.

New compounds

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Page/Page column 4; 9, (2008/06/13)

The present invention relates to new compounds of formula I, where R1 and R2 are independently halo or C1-3haloalkyl, X is ethenyl or ethynyl, or a salt thereof.

USE OF SPIRO [ IMIDAZOLIDINE-4, 3'-INDOLE] 2, 2', 5' (1H) TRIONES FOR TREATMENT OF CONDITIONS ASSOCIATED WITH VANILLOID RECEPTOR 1

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Page/Page column 26, (2008/06/13)

The present invention relates to a new use of spiro-hydantoin derivatives of formula (I), or salts, solvates or solvated salts thereof, as well as to new compounds, a process for their preparation and new intermediates used in the preparation thereof, pha

NEW COMPOUNDS I

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Page/Page column 26, (2008/06/13)

The present invention relates to new compounds of formula (I), wherein R1 to R9 and X are as defined as in formula I, or salts, solvates or solvated salts thereof, processes for their preparation and to new intermediates used in the

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