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2-[(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)methoxy]ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86625-99-2

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86625-99-2 Usage

Type of compound

chemical compound

Activities

antiviral and antineoplastic

Target enzymes

human immunodeficiency virus (HIV) and human T-lymphotropic virus type I (HTLV-I) reverse transcriptase

Classification

nucleoside analog

Function

potent inhibitor of reverse transcriptase

Potential applications

treatment of HIV and other viral infections, certain types of cancer

Status

experimental drug

Effectiveness

has shown promise in vitro and in animal studies

Check Digit Verification of cas no

The CAS Registry Mumber 86625-99-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,2 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86625-99:
(7*8)+(6*6)+(5*6)+(4*2)+(3*5)+(2*9)+(1*9)=172
172 % 10 = 2
So 86625-99-2 is a valid CAS Registry Number.

86625-99-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-aminopyrrolo[2,3-d]pyrimidin-7-yl)methoxy]ethanol

1.2 Other means of identification

Product number -
Other names 7-[2-Hydroxyethoxymethyl]-4-aminopyrrolo[2,3-d]pyrimidine

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:86625-99-2 SDS

86625-99-2Relevant academic research and scientific papers

Synthesis and antiviral activity of certain 4-substituted and 2,4-disubstituted 7-[(2-hydroxyethoxy)methyl]pyrrolo[2,3-d]pyrimidines

Saxena,Hagenow,Genzlinger,Turk,Drach,Townsend

, p. 1501 - 1506 (1988)

Treatment of the sodium salt of 4-chloro-2-(methylthio)pyrrolo[2,3-d]pyrimidine (2) with (2-acetoxyethoxy)methyl bromide (3) has provided 4-chloro-2-(methylthio)-7-[2-acetoxyethoxy)methyl]pyrrolo[2,3-d]pyrim dine (4). Ammonolysis of 4 at room temperature

Preparation of 7-Substituted Pyrrolopyrimidines and 9-Substituted Purines as Potential Antiparasitic Agents

LaMontagne, Maurice P.,Smith, David C.,Wu, Geng-Shuen

, p. 295 - 299 (2007/10/02)

A series of six 7-substituted pyrrolopyrimidines and two 9-substituted purines were prepared and evaluated for potential antiparasitic activity.All were inactive against P. berghei in mice.Six of the target compounds were also evaluated for antitrypanosomal activity against T. rhodensiense in mice.All six compounds were also inactive in this screen.

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