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1199828-99-3

methyl 1-(benzyloxycarbonylamino)-2,3-dihydro-1H-indene-5-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • methyl 1-(benzyloxycarbonylamino)-2,3-dihydro-1H-indene-5-carboxylate

    Cas No: 1199828-99-3

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  • 1199828-99-3 Structure

  • Basic information

    1. Product Name: methyl 1-(benzyloxycarbonylamino)-2,3-dihydro-1H-indene-5-carboxylate
    2. Synonyms: methyl 1-(benzyloxycarbonylamino)-2,3-dihydro-1H-indene-5-carboxylate
    3. CAS NO:1199828-99-3
    4. Molecular Formula:
    5. Molecular Weight: 325.364
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1199828-99-3.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: methyl 1-(benzyloxycarbonylamino)-2,3-dihydro-1H-indene-5-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 1-(benzyloxycarbonylamino)-2,3-dihydro-1H-indene-5-carboxylate(1199828-99-3)
    11. EPA Substance Registry System: methyl 1-(benzyloxycarbonylamino)-2,3-dihydro-1H-indene-5-carboxylate(1199828-99-3)

  • 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: 1199828-99-3(Hazardous Substances Data)

1199828-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1199828-99-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,9,8,2 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1199828-99:
(9*1)+(8*1)+(7*9)+(6*9)+(5*8)+(4*2)+(3*8)+(2*9)+(1*9)=233
233 % 10 = 3
So 1199828-99-3 is a valid CAS Registry Number.

1199828-99-3Relevant articles and documents

Structure based evolution of a novel series of positive modulators of the AMPA receptor

Jamieson, Craig,MacLean, John K.F.,Brown, Christopher I.,Campbell, Robert A.,Gillen, Kevin J.,Gillespie, Jonathan,Kazemier, Bert,Kiczun, Michael,Lamont, Yvonne,Lyons, Amanda J.,Moir, Elizabeth M.,Morrow, John A.,Pantling, John,Rankovic, Zoran,Smith, Lynn

scheme or table, p. 805 - 811 (2011/02/27)

Starting from compound 1, we utilized biostructural data to successfully evolve an existing series into a new chemotype with a promising overall profile, exemplified by 19.

INDANE DERIVATIVES

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Page/Page column 43-44, (2010/11/03)

The present invention relates to anindane derivative according to formula I wherein the variables are defined as in the specification, or to a pharmaceutically acceptable salt or solvate thereof. The present invention also relates to a pharmaceutical composition comprising one or more of said indane derivatives and to their use in therapy, for instance in the treatment or prevention of psychiatric diseases where an enhancement of synaptic responses mediated by AMPA receptors is required, including schizophrenia, depression and Alzheimer' s disease.

INDANE DERIVATIVES AS AMPA RECEPTOR MODULATORS

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, (2009/12/28)

The present invention relates to a heterocyclic derivative according to formula (I); wherein the variables are defined as in the specification, or to a pharmaceutically acceptable salt or solvate thereof. The present invention also relates to a pharmaceut

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