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1H-Purin-6-amine, 2-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1445-08-5

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1445-08-5 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 36, p. 3211, 1971 DOI: 10.1021/jo00820a029

Check Digit Verification of cas no

The CAS Registry Mumber 1445-08-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,4 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1445-08:
(6*1)+(5*4)+(4*4)+(3*5)+(2*0)+(1*8)=65
65 % 10 = 5
So 1445-08-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N5/c1-3-10-5(7)4-6(11-3)9-2-8-4/h2,4H,1H3,(H2,7,8,9,10,11)

1445-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-7H-purin-6-amine

1.2 Other means of identification

Product number -
Other names 1H-Purin-6-amine,2-methyl

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:1445-08-5 SDS

1445-08-5Relevant academic research and scientific papers

Gene therapy of cancer: activation of nucleoside prodrugs with e. colipurine nucleoside phosphorylase

Secrist III, John A.

, p. 745 - 757 (2007/10/03)

During the last few years, many gene therapy strategies have been developed for various disease targets. The development of anticancer gene therapy strategies to selectively generate cytotoxic nucleoside or nucleotide analogs is an attractive goal. One such approach involves the delivery of herpes simplex virus thymidine kinase followed by the acyclic nucleoside analog ganciclovir. We have developed another gene therapy methodology for the treatment of cancer that has several significant attributes. Specifically, our approach involves the delivery of E. coli purine nucleoside phosphorylase, followed by treatment with a relatively non-toxic nucleoside prodrug that is cleaved by the enzyme to a toxic compound. .This presentation describes the concept, details our search for suitable prodrugs, and summarizes the current biological data. Copyright

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