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Home > Encyclopedia > 5-Bromocytosine

5-Bromocytosine

5-Bromocytosine structure

5-Bromocytosine 

structure
  • CAS No:

    2240-25-7

  • Formula:

    C4H4BrN3O

  • Chemical Name:

    5-Bromocytosine

  • Synonyms:

    2(1H)-Pyrimidinone,6-amino-5-bromo-;Cytosine,5-bromo-;2(1H)-Pyrimidinone,4-amino-5-bromo-;6-Amino-5-bromo-2(1H)-pyrimidinone;5-Bromocytosine;4-Amino-5-bromo-2-hydroxypyrimidine;31295-39-3

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

LIGHT YELLOW AMORPHOUS POWDER

5-Bromocytosine Basic Attributes

190

190.00

218-806-8

2737MSZ714

DTXSID60176932

2933599090

Characteristics

67.5

-0.3

White to yellow Solid

1.3±0.1 g/cm3

245-255 °C (decomp)

171.2±27.9 °C

1.583

Soluble in formic acid (50 mg/ml).

Safety Information

NONH for all modes of transport

3

22-37/38-41-43-48-20/21/22

24/25-22-36/37/39-26-45-7/8

Xn

P261-P280-P305 + P351 + P338

H302-H315-H317-H318-H335

|Danger|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P272, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P330, P332+P313, P333+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 39 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

5-bromocytosine

5-Bromocytosine Use and Manufacturing

The cytosine (55.6g, 0.5mol), N-bromosuccinimide (106.8g, 0 . 6mol) and DMF150mL in added in the reaction bottle, cooling to 15 °C ultrasonic reaction 1h, TLC raw material the reaction is complete, filtering, the filter cake is washed with water (20 ml × 2) washing, drying to obtain 5-bromocytosine (90.9g, 95.6percent).The cytosine (55.6g, 0.5mol), N-bromosuccinimide (106.8g, 0 . 6mol) and DMF150mL in added in the reaction bottle, cooling to 15 °C ultrasonic reaction 1h, TLC raw material the reaction is complete, filtering, the filter cake is washed with water (20 ml × 2) washing, drying to obtain 5-bromocytosine (90.9g, 95.6percent). (95g, 0.5 mol), acetic anhydride (306.3g, 3mol) added to the reaction flask, the reaction was warmed to 70 °C 4h, the solvent was distilled off under reduced pressure, was added 200mL of methanol was heated to reflux for 30min, cooled to room temperature, filtered, the filter cake was washed with 30mL of methanol, and drying to give N-acetyl-The remainder of the transformations are carried out substantially as described to produce first the corresponding 1-(3, 5-di-O-benzoyl-2-deoxy-2-fluoro-beta-D-arabinofuranosyl)pyrimidine derivative and thereafter the 1-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)pyrimidine derivative....5-fluorouracil, 6-azathymine, A mixture of compound

Computed Properties

Molecular Weight:190.00
XLogP3:-0.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Exact Mass:188.95377
Monoisotopic Mass:188.95377
Topological Polar Surface Area:67.5
Heavy Atom Count:9
Complexity:208
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Material

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