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N4-Acetylcytosine

N4-Acetylcytosine Structure
CAS No.
14631-20-0
Chemical Name:
N4-Acetylcytosine
Synonyms
N-(2-Oxo-1,2-dihydropyriMidin-4-yl)acetaMide;N-ACETYLCYTOSINE;N4-AcetyL;N-Acetocytosine;N-Actyl cytosine;N4-ACETYLCYTOSINE;N4-Acetylcytosine 99%;N4-Acetylcytosine >LABOTEST-BB LT00012625;N(sup 4)-acetylcytosine
CBNumber:
CB5174391
Molecular Formula:
C6H7N3O2
Molecular Weight:
153.14
MOL File:
14631-20-0.mol
Modify Date:
2023/11/15 17:17:25

N4-Acetylcytosine Properties

Melting point >300 °C (lit.)
Density 1.41±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility DMSO (Sparingly), Methanol (Very Slightly)
pka 7.60±0.10(Predicted)
form Solid
color Off-White to Pale Beige
BRN 138451
InChI InChI=1S/C6H7N3O2/c1-4(10)8-5-2-3-7-6(11)9-5/h2-3H,1H3,(H2,7,8,9,10,11)
InChIKey IJCKBIINTQEGLY-UHFFFAOYSA-N
SMILES C(NC1=CC=NC(=O)N1)(=O)C
CAS DataBase Reference 14631-20-0(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  22-24/25-37/39-26-37
WGK Germany  3
HS Code  29335995
NFPA 704
1
2 0

N4-Acetylcytosine price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 377910 N4-Acetylcytosine 99% 14631-20-0 25G ₹11333.78 2022-06-14 Buy
TCI Chemicals (India) A2089 N4-Acetylcytosine 14631-20-0 5G ₹2200 2022-05-26 Buy
TCI Chemicals (India) A2089 N4-Acetylcytosine 14631-20-0 25G ₹6700 2022-05-26 Buy
Product number Packaging Price Buy
377910 25G ₹11333.78 Buy
A2089 5G ₹2200 Buy
A2089 25G ₹6700 Buy

N4-Acetylcytosine Chemical Properties,Uses,Production

Chemical Properties

Crstalline powder

Uses

N4-Acetylcytosine may be used in the preparation of cytidine. It may be used in the preparation of 1-(4-azido-4-deoxy-β-D-glucopyranosyl)cytosine.

General Description

Four stable conformers of N4-acetylcytosine, and the one of the stable form containing an intramoleuclar six-membered ring have been reported by theoretical calculations.The infrared and FT-Raman spectra of N4-acetylcytosine in the solid phase has been reported.

Purification Methods

If TLC or paper chromatography shows that it contains unacetylated cytosine, then reflux it in Ac2O for 4hours, cool at 3-4o for a few days, collect the crystals, wash them with cold H2O, then EtOH and dry at 100o. It is insoluble in EtOH and dissolves in H2O with difficulty, but crystallises in prisms from hot H2O. It is hydrolysed by 80% aqueous AcOH at 100o/1hour. [UV: Brown et al. J Chem Soc 2384 1956, Codington et al. J Am Chem Soc 80 5164 1958.] It forms an Hg salt [Fox et al. J Am Chem Soc 79 5060 1957]. [Beilstein 25 III/IV 3657.]

N4-Acetylcytosine Preparation Products And Raw materials

Global( 358)Suppliers
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JSK Chemicals +919879767970 Gujarat, India 3756 58 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
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Biopharmacule Speciality Chemicals P Ltd (India) +91 40 6462 1866 Hyderabad, India 526 58 Inquiry
AVIK PHARMACEUTICAL LIMITED +91-22-67685000 New Delhi, India 54 58 Inquiry
n-(1,2-dihydro-2-oxo-4-pyrimidinyl)-acetamid N4-ACETYLCYTOSINE LABOTEST-BB LT00012625 4-Acetylamino-2-hydroxypyrimidine N-Acetocytosine N(4)-Acetylcytosine,98% N-Actyl cytosine N(sup 4)-acetylcytosine 4-(Acetylamino)pyrimidine-2(1H)-one N-(2-Oxo-1,2-dihydropyrimidine-4-yl)acetamide N-[(2-Oxo-1,2-dihydropyrimidine)-4-yl]acetamide N-(2-keto-1H-pyrimidin-6-yl)acetamide N-(2-oxo-1H-pyrimidin-6-yl)acetamide N-(2-oxo-1H-pyrimidin-6-yl)ethanamide N4-Acetylcytosine N4-Acetylcytosine≥ 99% (HPLC) N4-Acetylcytosine 99% N-(2-oxo-2,3-dihydropyrimidin-4-yl)acetamide N4-Acetylcytosine USP/EP/BP Acetamide, N-(2,3-dihydro-2-oxo-4-pyrimidinyl)- N4-AcetyL N4-Acetylcytosine > N-(2-Oxo-1,2-dihydro-4-pyrimidinyl)acetamide N-ACETYLCYTOSINE N-(2-Oxo-1,2-dihydropyriMidin-4-yl)acetaMide 14631-20-0 Building Blocks Pyrimidines Heterocyclic Building Blocks Heterocyclic Compounds Building Blocks Heterocyclic Building Blocks Pyrimidines Biochemistry Nucleobases and their analogs Nucleosides, Nucleotides & Related Reagents