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24605-23-0

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24605-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24605-23-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,0 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24605-23:
(7*2)+(6*4)+(5*6)+(4*0)+(3*5)+(2*2)+(1*3)=90
90 % 10 = 0
So 24605-23-0 is a valid CAS Registry Number.

24605-23-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-5-methoxycyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-chloro-5-methoxybenzoquinone

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:24605-23-0 SDS

24605-23-0Relevant articles and documents

ONO-pincer ruthenium complex-bound norvaline for efficient catalytic oxidation of methoxybenzenes with hydrogen peroxide

Yoshida, Ryota,Isozaki, Katsuhiro,Yokoi, Tomoya,Yasuda, Nobuhiro,Sadakane, Koichiro,Iwamoto, Takahiro,Takaya, Hikaru,Nakamura, Masaharu

supporting information, p. 7468 - 7479 (2016/08/16)

The enhanced catalytic activity of ruthenium complex-bound norvaline Boc-l-[Ru]Nva-OMe 1, in which the ONO-pincer ruthenium complex Ru(pydc)(terpy) 2 is tethered to the α-side chain of norvaline, has been demonstrated for the oxidation of methoxybenzenes to p-benzoquinones with a wide scope of substrates and unique chemoselectivity.

Multistep Reversible Redox Systems, LXIII. 2,5-Disubstituted N,N'-Dicyanoquinone Diimines (DCNQIs) - Syntheses, and Redox Properties

Huenig, Siegfried,Bau, Robert,Kemmer, Martina,Meixner, Hubert,Metzenthin, Tobias,et al.

, p. 335 - 348 (2007/10/03)

Quinones 1a-q and DCNQIs 2a-g have been synthesized in order to investigate substituent effects.It was necessary to employ novel synthetic routes for the introduction of iodine into 1f (7), the trifluoromethyl group into 1g-i, deuterium into 1m-p, and esp

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