Welcome to LookChem.com Sign In|Join Free

CAS

  • or

65499-42-5

Post Buying Request

65499-42-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

65499-42-5 Usage

Type

Synthetic nucleoside analog of thymidine

Purpose

Antiretroviral medication for the treatment of HIV/AIDS

Mechanism of Action

Inhibits the reverse transcriptase enzyme, essential for HIV replication

Usage

Often used in combination with other antiretroviral drugs

Administration

Available in various formulations (capsules, oral solution) and taken orally

Side Effects

Potential side effects include peripheral neuropathy, pancreatitis, and lactic acidosis

Precaution

It is important to take stavudine as prescribed by a healthcare professional to optimize effectiveness and minimize adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 65499-42-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,9 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65499-42:
(7*6)+(6*5)+(5*4)+(4*9)+(3*9)+(2*4)+(1*2)=165
165 % 10 = 5
So 65499-42-5 is a valid CAS Registry Number.

65499-42-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-acetyloxy-5-[2,4-dioxo-5-(trifluoromethyl)pyrimidin-1-yl]oxolan-2-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names 3',5'-Di-O-Acetyl-5-trifluormethyl-desoxyuridin (4)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65499-42-5 SDS

65499-42-5Downstream Products

65499-42-5Relevant articles and documents

-

Kobayashi et al.

, p. 536 (1977)

-

Synthesis of nucleoside-based antiviral drugs in ionic liquids

Kumar, Vineet,Malhotra, Sanjay V.

supporting information; experimental part, p. 5640 - 5642 (2009/06/18)

Nucleoside-based antiviral drugs have been synthesized using imidazolium-based ionic liquids as reaction medium. The ionic liquids were proved to be better solvents for all the nucleoside in terms of solubility and reaction medium as compared to conventional molecular solvents.

Enzymatic regioselective acylation of the 3′-hydroxyl groups of 2′-deoxy-5-fluorouridine (FUdR) and 2′-Deoxy-5-trifiuoromethyluridine (CF3UdR)

Nozaki, Kenji,Uemura, Atuhiko,Yamashita, Jun-Ichi,Yasumoto, Mitsugi

, p. 7327 - 7328 (2007/10/02)

A lipase from Pseudomonas sp. (Amano PS) catalyzes regioselecfive acylation of the 3′-hydroxyl groups of FUdR and CF3UdR.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 65499-42-5