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2-chloro-3-{[2-(diethylamino)ethyl]amino}naphthalene-1,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69895-75-6

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69895-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69895-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,9 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69895-75:
(7*6)+(6*9)+(5*8)+(4*9)+(3*5)+(2*7)+(1*5)=206
206 % 10 = 6
So 69895-75-6 is a valid CAS Registry Number.

69895-75-6SDS

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-chloro-3-[2-(diethylamino)ethylamino]naphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-chloro-3-{[2-(diethylamino)ethyl]amino}naphthoquinone

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:69895-75-6 SDS

69895-75-6Downstream Products

69895-75-6Relevant academic research and scientific papers

Reactions of Substituted Indoles with 2,3-Dichloro-1,4-naphthoquinone and Electrochemical Properties of Some 2,3-Substituted 1,4-Naphthoquinones

Ibis,Ayla, S. Sahinler,Tulegenova,Bahar

, p. 546 - 553 (2019)

The reactions of 2,3-dichloro-1,4-naphthoquinone with some indoles and thiols were investigated. The resulting nucleophilic substitution products were characterized by spectroscopic methods (FT-IR, 1H and 13C NMR, MS) and microanalys

Composition for Distructing Microalgae

-

Paragraph 0414-0417, (2017/09/05)

The present invention relates to a composition for destroying microalgae, more specifically, to a composition for destroying microalgae containing naphthoquinone compounds having a specific exchange group. The composition for destroying microalgae, according to the present invention, can prevent green tide and red tide by being processed in areas such as cultivation facilities for microalgae, areas in which the green tide or the red tide occur, or areas expected to occur the green tide or the red tide.

Dioxonaphthoimidazoliums are Potent and Selective Rogue Stem Cell Clearing Agents with SOX2-Suppressing Properties

Ho, Si-Han Sherman,Ali, Azhar,Ng, Yi-Cheng,Lam, Kuen-Kuen Millie,Wang, Shu,Chan, Woon-Khiong,Chin, Tan-Min,Go, Mei-Lin

supporting information, p. 1944 - 1955 (2016/10/06)

Pluripotent stem cells are uniquely positioned for regenerative medicine, but their clinical potential can only be realized if their tumorigenic tendencies are decoupled from their pluripotent properties. Deploying small molecules to remove remnant undifferentiated pluripotent cells, which would otherwise transform into teratomas and teratomacarcinomas, offers several advantages over non-pharmacological methods. Dioxonapthoimidazolium YM155, a survivin suppressant, induced selective and potent cell death of undifferentiated stem cells. Herein, the structural requirements for stemotoxicity were investigated and found to be closely aligned with those essential for cytotoxicity in malignant cells. There was a critical reliance on the quinone and imidazolium moieties but a lesser dependence on ring substituents, which served mainly to fine-tune activity. Several potent analogues were identified which, like YM155, suppressed survivin and decreased SOX2 in stem cells. The decrease in SOX2 would cause an imbalance in pluripotent factors that could potentially prompt cells to differentiate and hence decrease the risk of aberrant teratoma formation. As phosphorylation of the NF-κB p50 subunit was also suppressed, the crosstalk between phospho-p50, SOX2, and survivin could implicate a causal role for NF-κB signaling in mediating the stem cell clearing properties of dioxonaphthoimidazoliums.

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