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ethyl (5-amino-2-methyl-3-phenyl-1,2-dihydropyrido[3,4-b]pyrazin-7-yl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 122293-95-2 Structure
  • Basic information

    1. Product Name: ethyl (5-amino-2-methyl-3-phenyl-1,2-dihydropyrido[3,4-b]pyrazin-7-yl)carbamate
    2. Synonyms: carbamic acid, N-(5-amino-1,2-dihydro-2-methyl-3-phenylpyrido[3,4-b]pyrazin-7-yl)-, ethyl ester
    3. CAS NO:122293-95-2
    4. Molecular Formula: C17H19N5O2
    5. Molecular Weight: 325.3651
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122293-95-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 483°C at 760 mmHg
    3. Flash Point: 245.9°C
    4. Appearance: N/A
    5. Density: 1.36g/cm3
    6. Vapor Pressure: 1.74E-09mmHg at 25°C
    7. Refractive Index: 1.671
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: ethyl (5-amino-2-methyl-3-phenyl-1,2-dihydropyrido[3,4-b]pyrazin-7-yl)carbamate(CAS DataBase Reference)
    11. NIST Chemistry Reference: ethyl (5-amino-2-methyl-3-phenyl-1,2-dihydropyrido[3,4-b]pyrazin-7-yl)carbamate(122293-95-2)
    12. EPA Substance Registry System: ethyl (5-amino-2-methyl-3-phenyl-1,2-dihydropyrido[3,4-b]pyrazin-7-yl)carbamate(122293-95-2)
  • 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: 122293-95-2(Hazardous Substances Data)

122293-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122293-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,2,9 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 122293-95:
(8*1)+(7*2)+(6*2)+(5*2)+(4*9)+(3*3)+(2*9)+(1*5)=112
112 % 10 = 2
So 122293-95-2 is a valid CAS Registry Number.

122293-95-2Downstream Products

122293-95-2Relevant articles and documents

Chiral ethyl [6-amino-4-[[12-(methoxymethylamino)-1-methyl-2-oxoethyl]amino]-5-nitro-2-pyridyl]carbamate

-

, (2008/06/13)

The present invention relates to compounds of the formula STR1 wherein each of R and R1 is a lower alkyl group having from 1 to 4 carbon atoms, which are useful as intermediates to make chiral ethyl (5-amino-1,2-dihydro-2-methyl-3-phenylpyrido[

New Anticancer Agents: Chiral Isomers of Ethyl 5-Amino-1,2-dihydro-2-methyl-3-phenylpyridopyrazine-7-carbamate

Temple, Carroll,Rener, Gregory

, p. 2089 - 2092 (2007/10/02)

Racemic ethyl 5-amino-1,2-dihydro-2-methyl-3-phenylpyridopyrazine-7-carbamate (1a) has shown antitumor activity in a variety of in vivo experiments.The preparation of the R (9) and S (10) isomers gave compounds with significant differences in potency in several biological tests.

'(2S)-(5-amino-1,2-dihydro-2-methyl-3-phenylpyrido(3,4-b)pyrazin-7-yl)-carbamic acid, ethyl ester

-

, (2008/06/13)

The (2S)-(-)-isomer of (5-amino-1,2-dihydro-2-methyl-3-phenylpyrido[3,4-b]pyrazin-7-yl)arbamic acid, ethyl ester is significantly more potent than either the (2R)-(+)-isomer or the (R,S)-(±)- racemic mixture in inhibiting mitotic cell division of L1210 leukemia cells. The compound, pharmaceutical compositions containing the compound, and a method of ameliorating cancer diseases in mammals are disclosed.

1,2-Dihydropyrido[3,4-b]pyrazines: Structure-activity relationships

Temple Jr.,Wheeler,Elliott,Rose,Comber,Montgomery

, p. 91 - 95 (2007/10/02)

Certain derivatives containing the 1,2-dihydropyrido[3,4-b]pyrazine (1-deaza-7,8-dihydropteridine) ring system are active against experimental neoplasms in mice. The mechanism of action of these agents has r539w1 =4-amino-1-deaza-7,8-dihydro-6-[(N-methyla

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