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64127-00-0

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64127-00-0 Usage

Classification

Potent alkylating agent

Uses

Chemotherapy for various types of cancer including brain tumors, lymphoma, and lung cancer

Mechanism of action

Damages DNA of cancer cells, inhibiting growth and proliferation

Administration

Oral

Absorption

Well-absorbed into bloodstream

Side effects

Myelosuppression, liver toxicity, pulmonary fibrosis

Importance

Important part of cancer therapy, often used in combination with other anticancer drugs

Check Digit Verification of cas no

The CAS Registry Mumber 64127-00-0 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, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64127-00:
(7*6)+(6*4)+(5*1)+(4*2)+(3*7)+(2*0)+(1*0)=100
100 % 10 = 0
So 64127-00-0 is a valid CAS Registry Number.

64127-00-0SDS

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 6-chloro-9-(2-chloroethyl)purine

1.2 Other means of identification

Product number -
Other names 6-Chlor-9-<2-chlor-aethyl>-purin

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:64127-00-0 SDS

64127-00-0Downstream Products

64127-00-0Relevant articles and documents

Synthesis and Properties of Purinophanes: Relationship between the Magnitude of Hypochromism and Stacking Geometry of Purine Rings

Seyama, F.,Akahori, K.,Sakata, Y.,Misumi, S.,Aida, M.,Nagata, C.

, p. 2192 - 2201 (2007/10/02)

Twelve purinophanes 1-12, in which two purine rings are fixed with different modes of stacking by two or three polymethylene chains, have been prepared by either stepwise introduction of the linking chains or quasi-dimerization of disubstituted purine der

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