- Alkylamino derivatives of pyrazinamide: Synthesis and antimycobacterial evaluationServusova, Barbora; Paterova, Pavla; Mandikova, Jana; Kubicek, Vladimir; Kucera, Radim; et al, Bioorganic & Medicinal Chemistry Letters, 2014, 24(2), 450-453
Cas no 89323-09-1 (5-Aminopyrazine-2-carboxamide)
5-Aminopyrazine-2-carboxamide structure
Product Name:5-Aminopyrazine-2-carboxamide
CAS No:89323-09-1
MF:C5H6N4O
MW:138.127339839935
MDL:MFCD08705774
CID:711588
PubChem ID:12571036
Update Time:2024-10-26
5-Aminopyrazine-2-carboxamide Chemical and Physical Properties
Names and Identifiers
-
- 5-amino-2-Pyrazinecarboxamide
- 2-Pyrazinecarboxamide,5-amino-
- 5-AMINOPYRAZINE-2-CARBOXAMIDE
- 2-Amino-5-carbamoylpyrazine
- 4750AC
- 5-amino-pyrazine-2-carboxylic acid amide
- AK102768
- ST2411723
- 5-Amino-2-pyrazinecarboxamide (ACI)
- Pyrazinecarboxamide, 5-amino- (7CI, 9CI)
- W17933
- CHEMBL3105664
- AKOS006290280
- MFCD08705774
- DS-3936
- SCHEMBL2220140
- CS-W019230
- DA-01437
- DTXSID60502954
- 89323-09-1
- SY113486
- 5-Aminopyrazine-2-carboxamide
-
- MDL: MFCD08705774
- Inchi: 1S/C5H6N4O/c6-4-2-8-3(1-9-4)5(7)10/h1-2H,(H2,6,9)(H2,7,10)
- InChI Key: JAVGJSUOZDZWBY-UHFFFAOYSA-N
- SMILES: O=C(C1C=NC(N)=CN=1)N
Computed Properties
- Exact Mass: 138.05400
- Monoisotopic Mass: 138.05416083g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 10
- Rotatable Bond Count: 1
- Complexity: 138
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 94.9
- XLogP3: -1.4
Experimental Properties
- Density: 1.426±0.06 g/cm3 (20 oC 760 Torr),
- Melting Point: 277-279 oC (water )
- Solubility: Soluble (180 g/l) (25 o C),
- PSA: 94.89000
- LogP: 0.43920
5-Aminopyrazine-2-carboxamide Security Information
- Signal Word:Warning
- Hazard Statement: H315-H319-H335
- Warning Statement: P261-P305+P351+P338
- Storage Condition:Keep in dark place,Inert atmosphere,Room temperature
5-Aminopyrazine-2-carboxamide Customs Data
- HS CODE:2934999090
- Customs Data:
China Customs Code:
2934999090Overview:
2934999090. Other heterocyclic compounds. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to
Summary:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
5-Aminopyrazine-2-carboxamide Pricemore >>
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| Alichem | A099001122-1g |
5-Aminopyrazine-2-carboxamide |
89323-09-1 | 98% | 1g |
$299.25 | 2023-08-31 | |
| TRC | A630133-10mg |
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89323-09-1 | 10mg |
$ 50.00 | 2022-06-07 | ||
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89323-09-1 | 50mg |
$ 70.00 | 2022-06-07 | ||
| TRC | A630133-100mg |
5-Aminopyrazine-2-carboxamide |
89323-09-1 | 100mg |
$ 115.00 | 2022-06-07 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-FL351-100mg |
5-Aminopyrazine-2-carboxamide |
89323-09-1 | 98% | 100mg |
464CNY | 2021-05-08 | |
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2641CNY | 2021-05-08 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-FL351-250mg |
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985CNY | 2021-05-08 | |
| Fluorochem | 229277-250mg |
5-Aminopyrazine-2-carboxamide |
89323-09-1 | 95% | 250mg |
£89.00 | 2022-02-28 | |
| Fluorochem | 229277-1g |
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| Fluorochem | 229277-5g |
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£695.00 | 2022-02-28 |
5-Aminopyrazine-2-carboxamide Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Ammonia Solvents: Methanol , Water ; 30 min, 95 °C
Reference
Production Method 2
Reaction Conditions
1.1 Catalysts: Manganese oxide (MnO2) , Ruthenium Solvents: Water ; 3 h, 60 °C
Reference
- An efficient hydration of nitriles with ruthenium-supported heterogeneous catalyst in water under moderate conditionsHussain, Muhammad Asif; Choi, Eun Ju; Maqbool, Adnan ; Atif, Muhammad; Zeb, Hassan ; et al, Journal of Industrial and Engineering Chemistry (Amsterdam, 2021, 99, 187-195
Production Method 3
Reaction Conditions
1.1 Reagents: Cuprous cyanide Solvents: Ethanol , Water
1.2 Reagents: Hydrochloric acid Solvents: Water
1.3 Reagents: Hydrogen sulfide
1.4 Reagents: Sodium hydroxide Solvents: Water
1.5 Reagents: Hydrochloric acid Solvents: Water
1.2 Reagents: Hydrochloric acid Solvents: Water
1.3 Reagents: Hydrogen sulfide
1.4 Reagents: Sodium hydroxide Solvents: Water
1.5 Reagents: Hydrochloric acid Solvents: Water
Reference
- Pyrazine chemistry. IV. Bromination of 2-amino-3-carbomethoxypyrazineEllingson, R. C.; Henry, R. L., Journal of the American Chemical Society, 1949, 71, 2798-800
5-Aminopyrazine-2-carboxamide Raw materials
5-Aminopyrazine-2-carboxamide Preparation Products
5-Aminopyrazine-2-carboxamide Related Literature
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
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Xinhuan Wang,Shuangfei Cai,Cui Qi Analyst, 2017,142, 2500-2506
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Sowmyalakshmi Venkataraman RSC Adv., 2015,5, 73807-73813
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Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
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Goonay Yousefalizadeh,Shideh Ahmadi,Nicholas J. Mosey,Kevin G. Stamplecoskie Nanoscale, 2021,13, 242-252
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