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63637-61-6

Carbamic acid, [3-(2-aminophenyl)-3-oxopropyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Carbamic acid, [3-(2-aminophenyl)-3-oxopropyl]-, methyl ester

    Cas No: 63637-61-6

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  • 63637-61-6 Structure

  • Basic information

    1. Product Name: Carbamic acid, [3-(2-aminophenyl)-3-oxopropyl]-, methyl ester
    2. Synonyms:
    3. CAS NO:63637-61-6
    4. Molecular Formula: C11H14N2O3
    5. Molecular Weight: 222.244
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63637-61-6.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: Carbamic acid, [3-(2-aminophenyl)-3-oxopropyl]-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, [3-(2-aminophenyl)-3-oxopropyl]-, methyl ester(63637-61-6)
    11. EPA Substance Registry System: Carbamic acid, [3-(2-aminophenyl)-3-oxopropyl]-, methyl ester(63637-61-6)

  • 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: 63637-61-6(Hazardous Substances Data)

63637-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63637-61-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,3 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63637-61:
(7*6)+(6*3)+(5*6)+(4*3)+(3*7)+(2*6)+(1*1)=136
136 % 10 = 6
So 63637-61-6 is a valid CAS Registry Number.

63637-61-6Relevant articles and documents

A simple biomimetic synthesis of styelsamine B.

Skyler,Heathcock

, p. 4323 - 4324 (2001)

An extremely rapid, low cost, and environmentally friendly entry into the pyridoacridine family of alkaloids has been devised, as demonstrated here by the first total synthesis of styelsamine B (3) and its oxidation to the quinoneimine cystodytin J (4). T

Bioinspired Syntheses of the Pyridoacridine Marine Alkaloids Demethyldeoxyamphimedine, Deoxyamphimedine, and Amphimedine

Khalil, Iman M.,Barker, David,Copp, Brent R.

, p. 282 - 289 (2016/01/15)

Efficient bioinspired syntheses of the biologically active pyridoacridine marine alkaloids demethyldeoxyamphimedine, deoxyamphimedine, and amphimedine are reported. Reaction of styelsamine D, prepared via an optimized route starting from Boc-dopamine, wit

Synthesis, DNA binding and antitumor evaluation of styelsamine and cystodytin analogues

Fong, Hugo K.H.,Copp, Brent R.

, p. 274 - 299 (2013/05/21)

A series of N-14 sidechain substituted analogues of styelsamine (pyrido[4,3,2-mn]acridine) and cystodytin (pyrido[4,3,2-mn]acridin-4-one) alkaloids have been prepared and evaluated for their DNA binding affinity and antiproliferative activity towards a pa

REACTIVITY OF OXYTRIPTAMINE. CONVERSION TO 3-(o-AMINOPHENYL)-2-PYRROLIDONE AND KYNURENAMINE

Nakagawa, Masako,Maruyama, Takako,Hirakoso, Kazuyuki,Hino, Tohru

, p. 4839 - 4842 (2007/10/02)

Oxytriptamine 1 was converted to kynurenamine 5, benzooxazinone 6, and 3-hydroxy derivative 7b in NaOH-MeOH in the presence of oxygen, whereas 1 undergoes N,N'-transacylation to give the isomeric product 4 in argon atmosphere.

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