N-Acetyl cytosine structure
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Common Name | N-Acetyl cytosine | ||
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CAS Number | 14631-20-0 | Molecular Weight | 153.139 | |
Density | 1.4±0.1 g/cm3 | Boiling Point | N/A | |
Molecular Formula | C6H7N3O2 | Melting Point | >300 °C(lit.) | |
MSDS | Chinese USA | Flash Point | N/A |
Name | N4-Acetylcytosine |
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Synonym | More Synonyms |
Density | 1.4±0.1 g/cm3 |
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Melting Point | >300 °C(lit.) |
Molecular Formula | C6H7N3O2 |
Molecular Weight | 153.139 |
Exact Mass | 153.053833 |
PSA | 75.11000 |
LogP | -2.12 |
Index of Refraction | 1.625 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi: Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2933990090 |
~94% N-Acetyl cytosine CAS#:14631-20-0 |
Literature: Okabe; Sun; Zenchoff Journal of Organic Chemistry, 1991 , vol. 56, # 14 p. 4392 - 4397 |
~19% N-Acetyl cytosine CAS#:14631-20-0 |
Literature: Collection of Czechoslovak Chemical Communications, , vol. 47, # 11 p. 2961 - 2968 |
~% N-Acetyl cytosine CAS#:14631-20-0 |
Literature: Tetrahedron, , vol. 40, # 1 p. 125 - 135 |
~% N-Acetyl cytosine CAS#:14631-20-0 |
Literature: Journal of Organic Chemistry, , vol. 57, # 12 p. 3473 - 3478 |
Precursor 5 | |
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DownStream 5 | |
HS Code | 2933599090 |
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Summary | 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Synthesis and properties of N-(2, 3, 5-tri-O-acetyl-D-ribofuranosyl) maleimide. Schwartz AL and Lerner LM.
J. Org. Chem. 40(1) , 24-28, (1975)
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Molecular structure and vibrational spectra of N4-acetylcytosine.
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 112 , 139-45, (2013) The infrared and FT-Raman spectra of N4-acetylcytosine in the solid phase have been recorded, and the molecular geometrical parameters were optimized using B3LYP and MP2 methods with 6-311++G(d,p) bas... |
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Nucleosides. 63. Synthetic studies on nucleoside antibiotics. 3. Total synthesis of 1-(4-amino-4-deoxy-beta-d-glucopyranosyluronic acid)cytosine, the nucleoside moiety of gougerotin.
J. Org. Chem. 35(1) , 231-6, (1970)
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N-(2-Oxo-1,2-dihydropyrimidin-4-yl)acetamide |
Acetamide, N-(2,3-dihydro-2-oxo-4-pyrimidinyl)- |
N-(2-oxo-1H-pyrimidin-6-yl)acetamide |
N-(2-oxo-2,3-dihydropyrimidin-4-yl)acetamide |
MFCD00134466 |
N-(2-Oxo-2,3-dihydro-4-pyrimidinyl)acetamide |
N4-Acetylcytosine |