Welcome to LookChem.com Sign In|Join Free
  • or
Cyclopentanemethanol, 3-(6-amino-9H-purin-9-yl)-4-hydroxy-, (1S,3R,4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57345-50-3

Post Buying Request

57345-50-3 Suppliers

Recommended suppliers

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

57345-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57345-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,4 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57345-50:
(7*5)+(6*7)+(5*3)+(4*4)+(3*5)+(2*5)+(1*0)=133
133 % 10 = 3
So 57345-50-3 is a valid CAS Registry Number.

57345-50-3SDS

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 (1R,2R,4S)-2-(6-Amino-purin-9-yl)-4-hydroxymethyl-cyclopentanol

1.2 Other means of identification

Product number -
Other names -

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:57345-50-3 SDS

57345-50-3Downstream Products

57345-50-3Relevant academic research and scientific papers

(±)-3'-Deoxyaraaristeromycin via a surprising rearrangement

Frick,Patil,Gambino,Schneller

, p. 5541 - 5544 (1993)

Hydrolysis of (±)-3β-acetoxy-4α-benzamido-1α-cyclopentanemethyl acetate (5) with 6 N hydrochloric acid has been found to give an amine in which the configuration at C-3 has been inverted. This conclusion was reached following conversion of the amine into (±)-3'-deoxyaraaristeromycin (8) by following a standard adenine formation process of (i) reaction with 5-amino-4,6-dichloropyrimidine, (ii) ring closure with diethoxymethyl acetate, and (iii) ammonolysis. Use of basic hydrolysis conditions with 5 led to the expected (±)-3'-deoxyaristeromycin (7).

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 57345-50-3