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14937-67-8

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14937-67-8 Usage

Chemical Structure

Consists of a purine core with an amino group at the 2-position and a phenylethyl group at the 8-position

Classification

Heterocyclic compound

Potential Biological Activities

Acts as an adenosine receptor antagonist, regulates neurotransmission

Potential Therapeutic Uses

Being studied for Alzheimer's disease, Parkinson's disease, cancer

Other Investigated Roles

Modulates inflammation and immune responses

Promising Drug Target

Subject of ongoing research and shows potential as a therapeutic agent

Check Digit Verification of cas no

The CAS Registry Mumber 14937-67-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,3 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14937-67:
(7*1)+(6*4)+(5*9)+(4*3)+(3*7)+(2*6)+(1*7)=128
128 % 10 = 8
So 14937-67-8 is a valid CAS Registry Number.

14937-67-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-8-(2-phenylethyl)-3,7-dihydropurin-6-one

1.2 Other means of identification

Product number -
Other names 8-Phenaethyl-guanin

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:14937-67-8 SDS

14937-67-8Downstream Products

14937-67-8Relevant articles and documents

An improved procedure for the preparation of 8-substituted guanines

Xu, Ming,De Giacomo, Fabio,Paterson, Duncan E.,George, Tesmol G.,Vasella, Andrea

, p. 1452 - 1453 (2007/10/03)

The preparation of 8-substituted guanines using a new phosphorus(III)-mediated cyclisation of 4-acylamino-5-nitrosopyrimidines as the key step is described.

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