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N4-Acetylcytidine

N4-Acetylcytidine structure

N4-Acetylcytidine 

structure
  • CAS No:

    3768-18-1

  • Formula:

    C11H15N3O6

  • Chemical Name:

    N4-Acetylcytidine

  • Synonyms:

    Cytidine,N-acetyl-;Acetamide,N-(1,2-dihydro-2-oxo-1-β-D-ribofuranosyl-4-pyrimidinyl)-;N-Acetylcytidine;N4-Acetylcytidine;4-Acetylcytidine;N4-Acetylcytidine

  • Categories:

    Biochemical Engineering  >  Saccharides

Description

N4-Acetylcytidine is an endogenous metabolite.


Solid


N(4)-acetylcytidine is cytidine in which one of the exocyclic amino hydrogens is substituted by an acetyl group. It has a role as a metabolite. It is a member of cytidines, a member of acetamides and a secondary carboxamide.

N4-Acetylcytidine Basic Attributes

285.25

285.25

223-195-6

2934999090

Characteristics

132

-1.4

Solid

1.7±0.1 g/cm3

208-209 °C

1.699

−20°C

162.7 Ų [M+H]+ [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]|161.4 Ų [M-H]- [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]

Safety Information

3

20/21/22-36/37/38

36-36/37/39-26

Xn

P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, P501

H302

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, and P501|Aggregated GHS information provided by 2 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

4-acetylcytidine

N4-Acetylcytidine Use and Manufacturing

In a 500 mL three-necked flask was added 50.0 g of Compound 3 powder and 250 mL of acetonitrile and 25 mL of acetic anhydride, stirred and refluxed for 3 h, cooled to room temperature and filtered with suction. The solid was washed with acetonitrile twice and the filter cake was dried to give 56.3 g of compound 4 with a yield of 96.0 percent.To a solution of cytidine (1.22 g, 5.00 mmol) in DMF(40 mL) is added acetic anhydride (0.94 mL, 10.00 mmol). The solution is treated with microwave radiation (Panasonic, 1000 Watts) at full power for 40 seconds. The solution is concentrated in vacuo and the residue is co-evaporated with methanol (2.x.20 mL) to give 4-N-acetyl-cytidine (1.43 g, 95.0percent) as a white powder. MS (FAB):m/z 286 (MHCytidine (100.Og, 0.41 mol) was dissolved in DMF (500 ml), acetic anhydride (42.5 ml, 45.9 g, 0.45 mol) was added and the whole was left for 24 h. Solvent was evaporated, the residue boiled with methanol (40 ml) and cooled. Crystals were filtered and dried to furnish Λ^-acetylcytidine (102 g, 87.0percent).claim 1wherein the compound is...5-Fluorocytidine, 1-(beta-D -arabinofuranosyl)-5-fluorocytosine, 5-Methylcytidine, 2', 3'-Dideoxycytidine, N4-Acetylcytidine, 3'-Deoxycytidine, 4-Methoxy-1-(beta-D-ribofuranosyl)pyrimidin-2(1H)-one, 4-Methylthio-1-(beta-D-ribofuranosyl)pyrimidin-2(1H)-one, ...

Computed Properties

Molecular Weight:285.25
XLogP3:-1.4
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:285.09608521
Monoisotopic Mass:285.09608521
Topological Polar Surface Area:132
Heavy Atom Count:20
Complexity:477
Defined Atom Stereocenter Count:4
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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