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Phenol,4-[bis(2-chloroethyl)amino]-, hydrochloride (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1457-06-3

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1457-06-3 Usage

Uses

Used in Oncology:
Used in Cancer Research:
In addition to its clinical applications, Phenol, 4-[bis(2-chloroethyl)amino]-, hydrochloride (1:1) is also used in cancer research to study the mechanisms of action of alkylating agents and to develop new strategies for cancer treatment. Its cytotoxic properties make it a valuable tool for investigating the effects of DNA damage on cancer cells and for identifying potential targets for therapeutic intervention.
Used in Drug Development:
Phenol, 4-[bis(2-chloroethyl)amino]-, hydrochloride (1:1) serves as a starting point for the development of new anticancer drugs. Its unique chemical structure and alkylating properties provide a foundation for the design of novel compounds with improved selectivity, efficacy, and reduced toxicity. Researchers are working to modify the structure of Phenol,4-[bis(2-chloroethyl)amino]-, hydrochloride (1:1) to develop more targeted therapies that can selectively kill cancer cells while minimizing damage to healthy tissues.
Used in Drug Delivery Systems:
To overcome the limitations of Phenol, 4-[bis(2-chloroethyl)amino]-, hydrochloride (1:1), such as its high toxicity and side effects, researchers are developing drug delivery systems to improve its therapeutic index. These systems, which may include liposomes, nanoparticles, or other carriers, aim to enhance the delivery of the compound to cancer cells, increase its bioavailability, and reduce its impact on healthy tissues.

Check Digit Verification of cas no

The CAS Registry Mumber 1457-06-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,5 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1457-06:
(6*1)+(5*4)+(4*5)+(3*7)+(2*0)+(1*6)=73
73 % 10 = 3
So 1457-06-3 is a valid CAS Registry Number.

1457-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[bis(2-chloroethyl)amino]phenol,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-<N,N-bis(2-chloroethyl)amino>phenol hydrochloride

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:1457-06-3 SDS

1457-06-3Relevant academic research and scientific papers

HYPOXIA ACTIVATED DRUGS OF NITROGEN MUSTARD ALKYLATORS

-

, (2009/12/23)

Hypoxia activated drug compounds having a structure of formula(I) are useful in the treatment of cancer and other hyperproliferative diseases.

Melanocyte-directed enzyme prodrug therapy (MDEPT): Development of second generation prodrugs for targeted treatment of malignant melanoma

Jordan, Allan M.,Khan, Tariq H.,Malkin, Hugh,Osborn, Helen M.I.,Photiou, Andrew,Riley, Patrick A.

, p. 1549 - 1558 (2007/10/03)

Evaluation of second generation prodrugs for MDEPT, by oximetry, has highlighted structural properties that are advantageous and disadvantageous for efficient oxidation using mushroom tyrosinase. In particular, a sterically undemanding prodrug bis-(2-chlo

Melanocyte-directed enzyme prodrug therapy (MDEPT): Development of a targeted treatment for malignant melanoma

Jordan, Allan M.,Khan, Tariq H.,Osborn, Helen M. I.,Photiou, Andrew,Riley, Patrick A.

, p. 1775 - 1780 (2007/10/03)

A novel prodrug rationally designed to function as a tyrosinase substrate has been synthesised to allow targeted treatment of malignant melanoma. This agent has been evaluated for tyrosinase-mediated drug release, and has been shown to act in the desired

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