Welcome to LookChem.com Sign In|Join Free
  • or
7-Chloro-3-(2-hydroxyethyl)-1H-pyrazolo[4,3-d]pyriMidine, 97% is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64127-15-7

Post Buying Request

64127-15-7 Suppliers

Recommended suppliers

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

64127-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64127-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,2 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64127-15:
(7*6)+(6*4)+(5*1)+(4*2)+(3*7)+(2*1)+(1*5)=107
107 % 10 = 7
So 64127-15-7 is a valid CAS Registry Number.

64127-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(7-Chloro-3H-pyrazolo-[4,3-d]pyrimidin-3-yl)ethanol

1.2 Other means of identification

Product number -
Other names 2-(4-chloro-pyrazolo[3,4-d]pyrimidin-1-yl)-ethanol

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:64127-15-7 SDS

64127-15-7Relevant academic research and scientific papers

A short synthesis of 4-substituted 1-(hydroxyalkyl)-1H-pyrazolo[3,4-d]pyrimidines

Zacharie, Boulos,Connolly, Timothy P.,Rej, Rabindra,Attardo, Giorgio,Penney, Christopher L.

, p. 2271 - 2278 (2007/10/03)

A simple and practical procedure was developed for the preparation of 4-substituted-1-(hydroxyalkyl)-1H-pyrazolo[3,4-d]pyrimidines. This was achieved by reacting nucleobase 3a or 3b with cesium carbonate or DBU in the presence of various alkyl iodides at 0°C in DMF. This procedure appears to be of general utility, proceeds in reasonable yield, and is applicable to different alkyl chain lengths including protected and unprotected alcohols. The synthetic utility of this approach is demonstrated by the facile synthesis of ST 689, a potent immunostimulatory drug.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 64127-15-7