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Pyrazinecarboxylic acid, 3-amino-5-methyl- (7CI,8CI,9CI)

Detailed Information

  • Product Name:Pyrazinecarboxylic acid, 3-amino-5-methyl- (7CI,8CI,9CI)
  • CasNo.:6761-50-8
  • MF:C6H7N3O2
  • MW:153.14

pd_nature

  • Purity:99%
  • pd_boiling:211 °C
  • Packing:
  • Throughput:

Product Details;

CasNo: 6761-50-8

MF: C6H7N3O2

China cas 6761-50-8 manufacturer wholesale Pyrazinecarboxylic acid, 3-amino-5-methyl- (7CI,8CI,9CI) at affordable price

  • Molecular Formula:C6H7N3O2
  • Molecular Weight:153.14
  • Vapor Pressure:1.05E-06mmHg at 25°C 
  • Melting Point:211 °C 
  • Refractive Index:1.637 
  • Boiling Point:387.7 °C at 760 mmHg 
  • PKA:4.14±0.10(Predicted) 
  • Flash Point:188.3 °C 
  • PSA:89.10000 
  • Density:1.431 g/cm3 
  • LogP:0.64660 

Pyrazinecarboxylic acid, 3-amino-5-methyl- (7CI,8CI,9CI)(Cas 6761-50-8) Usage

General Description

Pyrazinecarboxylic acid, 3-amino-5-methyl- (7CI,8CI,9CI) is a chemical compound with the molecular formula C7H8N2O2. It is a derivative of pyrazinecarboxylic acid, with an amino group and a methyl group attached to the third and fifth carbon atoms, respectively. Pyrazinecarboxylic acid, 3-amino-5-methyl- (7CI,8CI,9CI) is often used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It has potential applications in the pharmaceutical industry, particularly in the development of new drugs and medical treatments. Additionally, it may also have uses in the fields of agriculture and chemical research. However, as with any chemical compound, proper handling and safety precautions should be observed when using pyrazinecarboxylic acid, 3-amino-5-methyl- to prevent potential hazards and health risks.

InChI:InChI=1/C6H7N3O2/c1-3-2-8-4(6(10)11)5(7)9-3/h2H,1H3,(H2,7,9)(H,10,11)

6761-50-8 Relevant articles

-

Cain et al.

, p. 3026,3028 (1948)

-

Organic compounds

-

Page/Page column 46, (2009/10/01)

The present invention concerns a compoun...

THIAZOLIUMS AS TRANSKETOLASE INHIBITORS

-

Page/Page column 39, (2008/06/13)

The present invention provides N-3'-pyri...

Research on heterocyclic compounds. XXXVII. Synthesis and antiinflammatory activity of methyl-substituted imidazo[1,2-a]pyrazine derivatives

Rimoli,Avallone,De Caprariis,Luraschi,Abignente,Filippelli,Berrino,Rossi

, p. 195 - 203 (2007/10/03)

A series of methyl-substituted imidazo[1...

6761-50-8 Process route

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7-methyl-1H-pteridine-2,4-dione

1-methyl-4-nitrosobenzene
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1-methyl-4-nitrosobenzene

5-methyl-3-oxo-3,4-dihydro-pyrazine-2-carboxylic acid
120992-57-6

5-methyl-3-oxo-3,4-dihydro-pyrazine-2-carboxylic acid

2-amino-6-methylpyrazine-3-carboxylic acid
6761-50-8

2-amino-6-methylpyrazine-3-carboxylic acid

Conditions
Conditions Yield
at 180 - 190 ℃;
7-methyl-pteridine-2,4-diol
13401-38-2

7-methyl-pteridine-2,4-diol

2-amino-6-methylpyrazine-3-carboxylic acid
6761-50-8

2-amino-6-methylpyrazine-3-carboxylic acid

Conditions
Conditions Yield
7-methyl-pteridine-2,4-diol; With sodium hydroxide; In water; for 96h; Heating / reflux;
With hydrogenchloride; In water; pH=1.5;
43%
With sodium hydroxide; In water; for 20h; Heating;
30%
7-methyl-pteridine-2,4-diol; With water; sodium hydroxide; at 150 ℃; for 72h;
With hydrogenchloride; In water; at 20 ℃; pH=2.5;

6761-50-8 Upstream products

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    7-methyl-2,4-diaminopteridine

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    7-methyl-1H-pteridine-2,4-dione

6761-50-8 Downstream products

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    sulfanilic acid-(6-methyl-pyrazin-2-ylamide)

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    (3-amino-5-methylpyrazin-2-yl)methanol

  • 74290-69-0
    74290-69-0

    (5-bromo-6-methyl-pyrazin-2-yl)amine

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