ChemicalBook > CAS DataBase List > Brivudine

Brivudine

Product Name
Brivudine
CAS No.
69304-47-8
Chemical Name
Brivudine
Synonyms
BVDU;BVDR;BrVDU;Helpin;Brivudin;SC-38394;BRIVUDINE;Brivudine BVdU;Brivudine USP/EP/BP;Bromovinyldeoxyuridine
CBNumber
CB6143433
Molecular Formula
C11H13BrN2O5
Formula Weight
333.14
MOL File
69304-47-8.mol
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Brivudine Property

Melting point:
165°C
Density 
1.7800 (rough estimate)
refractive index 
1.6520 (estimate)
storage temp. 
Inert atmosphere,2-8°C
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
pka
8.37±0.10(Predicted)
color 
Off-White
Water Solubility 
Soluble in water and methanol.
Merck 
14,1378
InChIKey
ODZBBRURCPAEIQ-CXYVBZRVSA-N
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Safety

Safety Statements 
24/25
WGK Germany 
3
RTECS 
YU7355000
HS Code 
29349990
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SBR00107
Product name
Brivudine
Purity
≥95%
Packaging
1 unit
Price
$57.7
Updated
2025/07/31
Sigma-Aldrich
Product number
B9647
Product name
(E)-5-(2-Bromovinyl)-2′-deoxyuridine
Packaging
10mg
Price
$344
Updated
2025/07/31
TCI Chemical
Product number
B3404
Product name
(E)-5-(2-Bromovinyl)-2'-deoxyuridine
Purity
>98.0%(HPLC)(T)
Packaging
100mg
Price
$121
Updated
2025/07/31
Cayman Chemical
Product number
29448
Product name
Brivudine
Packaging
100mg
Price
$97
Updated
2024/03/01
Cayman Chemical
Product number
29448
Product name
Brivudine
Packaging
1g
Price
$530
Updated
2024/03/01
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Brivudine Chemical Properties,Usage,Production

Description

(E)-5-(2-Bromovinyl)-2'-deoxyuridine is an thymidine analogue and acts as an anti-viral by inhibiting DNA plymerase.

Chemical Properties

White solid

Uses

It is used as pharmaceutical intermediate.

Uses

Brivudine is a nucloside analog which causes induction of neuronal differentiation in human reporter cell lines and adult stem cells. Anti-Herpes medication.

Synthesis

74131-06-9

69304-47-8

GENERAL STEPS: To a solution of (E)-5-(2-carboxyvinyl)-1-(2-deoxy-β-D-erythro-pentofuranosyl)pyrimidine-2,4(1H,3H)-dione (5.777 g, 19.37 mmol) in dimethylformamide (29 mL) was added K2CO3 (5.890 g, 42.61 mmol), and the suspension was stirred at room temperature for for 15 min. A solution of N-bromosuccinimide (3.655 g, 20.53 mmol) was added dropwise over a period of 30 min at 20 °C. After completion of the reaction, the resulting suspension was filtered and the solid was washed with DMF. The combined filtrate and washings were evaporated to dryness under vacuum and the residue was dissolved in methanol. Silica gel was added to this solution, the suspension was evaporated to dryness, and the solid was loaded onto the top of the column. Column chromatography using chloroform/methanol (92:8, v/v) as eluent gave a white solid (5.787 g, 71.9% yield). A white powder was obtained by recrystallization from water. The structure of the product was confirmed by 1H-NMR and 13C-NMR: 1H-NMR (DMSO-d6; 300 MHz) δ 11.59 (1H, bs, NH-3), 8.08 (1H, s, H-6), 7.25 (1H, d, 3J = 13.6 Hz, H-5B), 6.85 (1H, d, J = 13.6 Hz, H-5A) , 6.13 (1H, t, 3J = 6.5 Hz, H-1'), 5.29 (1H, bs, OH-3'), 5.13 (1H, bs, OH-5'), 4.24 (1H, m, H-3'), 3.79 (1H, m, H-4'), 3.66 (2H, m, H-5'), 2.51 (1H, m, H-2'), 2.14 (1H, m, H-2'); 13C-NMR (DMSO-d6; 75 MHz) δ 40.2 (C-2'), 61.3 (C-5'), 70.3 (C-4'), 84.8 (C-3'), 87.8 (C-1'), 108.9 (C-5B), 110.0 (C-5), 130.3 (C-5A), 149.6 , 162.1 (c-2, c-4).

in vivo

At a dose of 125 mg once daily, brivudine has proved to be superior to aciclovir with respect to reducing the period of new blister production, and has shortened the duration of post-herpetic neuralgia[1].

References

[1] Bioorganic and Medicinal Chemistry, 2005, vol. 13, # 24, p. 6663 - 6671
[2] RSC Advances, 2015, vol. 5, # 31, p. 24558 - 24563
[3] Patent: WO2005/12327, 2005, A2. Location in patent: Page/Page column 24-25
[4] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 20, p. 5640 - 5642
[5] Patent: US6653318, 2003, B1

Brivudine Preparation Products And Raw materials

Raw materials

Preparation Products

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Brivudine Suppliers

LGM Pharma
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1-(800)-881-8210
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inquiries@lgmpharma.com
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MedChemexpress LLC
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021-58955995
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Target molecule Corp.
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857-239-0968
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service1@targetmol.com
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TargetMol Chemicals Inc.
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marketing@targetmol.com
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BOC Sciences
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1-631-614-7828
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inquiry@bocsci.com
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Alchem Pharmtech,Inc.
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sales@alchempharmtech.com
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TargetMol Chemicals Inc.
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marketing@targetmol.com
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United States
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TargetMol Chemicals Inc.
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support@targetmol.com
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Aladdin Scientific
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Abcam Limited
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MedChemExpress
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Combi-Blocks Inc.
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3B Scientific Corporation
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View Lastest Price from Brivudine manufacturers

Henan Aochuang Chemical Co.,Ltd.
Product
Brivudine 69304-47-8
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1Ton
Release date
2022-09-29
R&D Scientific Inc.
Product
Brivudine 69304-47-8
Price
US $780.00/g
Min. Order
1g
Purity
95
Supply Ability
500 Kg
Release date
2024-04-26
Hangzhou ICH Biofarm Co., Ltd
Product
Brivudine 69304-47-8
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
99.0%
Supply Ability
20 tons
Release date
2023-07-13

69304-47-8, BrivudineRelated Search:


  • Helpin
  • Uridine,5-[(1E)-2-broMoethenyl]-2'-deoxy-
  • (E)-(5)-BROMOVINYL-2-DEOXYURIDINE
  • (<i>E</i>)-5-(2-Bromovinyl)-2'-deoxyuridine
  • BVDU
  • (E)-5-(2-BROMOVINYL)-2'-DEOXY-URIDINE
  • BRIVUDINE
  • 5-(E)-(2-Bromovinyl)-2-deoxyuridine
  • 5-(2-Bromovinyl)-deoxy-uridine
  • 5-[(E)-2-Bromoethenyl]-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione
  • Bromovinyldeoxyuridine
  • Brivudine BVdU
  • Brivudine(BroMovinyldeoxyuridine)
  • Brivudin
  • BrVDU
  • BVDR
  • SC-38394
  • BROMOVINYLDEOXYURIDINE; BVDU
  • (E)-5-(2-Bromovinyl)-2'-deoxyuridine &gt
  • 5-((E)-2-bromovinyl)-1-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione
  • Brivudine USP/EP/BP
  • BrivudineQ: What is Brivudine Q: What is the CAS Number of Brivudine Q: What is the storage condition of Brivudine Q: What are the applications of Brivudine
  • 5-[(1E)-2-bromoethenyl)-2'-deoxyuridine
  • (E)-5-(2-Bromovinyl)-2'-deoxyuridine
  • Barbituric Acid Impurity 19
  • Brivudine, pyrimidine nucleoside analog
  • Brivudine, 10 mM in DMSO
  • 69304-47-8
  • 69304-46-8
  • C11H13BrN2O5
  • C11H13BO5Rn2
  • Immune System Regulation
  • Immune Cell Signaling and Blood
  • Cell Signaling and Neuroscience
  • Cell Biology
  • BioChemical
  • AIDS and Viral Research Reagents
  • Inhibitors
  • API
  • 69304-47-8