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790-50-1

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790-50-1 Usage

Type of compound

Synthetic chemical compound with potential antineoplastic activity

Structural relation

Related to the chemotherapy drug Dacarbazine

Mechanism of action

Methylation of DNA at the O6 position of guanine, leading to DNA damage and apoptosis in rapidly dividing cells, particularly cancer cells

Potential use

Treatment of various solid tumors, such as brain tumors and melanoma

Treatment approach

May have potential in combination therapy with other chemotherapeutic agents

Current status

Further research and clinical trials are needed to fully understand its efficacy and safety profile.

Check Digit Verification of cas no

The CAS Registry Mumber 790-50-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,9 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 790-50:
(5*7)+(4*9)+(3*0)+(2*5)+(1*0)=81
81 % 10 = 1
So 790-50-1 is a valid CAS Registry Number.

790-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dichloro-N-[(2,4-dichlorophenyl)diazenyl]aniline

1.2 Other means of identification

Product number -
Other names 2,4,2',4'-tetrachlorodiazoaminobenzene

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:790-50-1 SDS

790-50-1Relevant articles and documents

Etude du Comportement Photochimique de quelques Diaryl-1,3-triazenes

Julliard, Michel,Vernin, Gaston,Metzger, Jacques

, p. 456 - 466 (2007/10/02)

The photolysis of Diaryl-1,3-triazenes gives products whose structures are consistent with a cage recombination process of homolytically formed radicals and subsequent abstraction of hydrogen from the solvent molecules by arylamino radicals.In aromatic solvents, a free-radical chain process leads to the formation of products resulting from the homolytic substitution on the solvent.Quenching experiments show that singlet and triplet excited states are reactive but that intersystem crossing efficiency is low.

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