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94042-08-7

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94042-08-7 Usage

Chemical Properties

Beige Solid

Uses

Oxaliplatin (O845075) intermediate as anti-cancer therapeutic agent and dual therapeutic/imaging contrast agent.

Check Digit Verification of cas no

The CAS Registry Mumber 94042-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,4 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 94042-08:
(7*9)+(6*4)+(5*0)+(4*4)+(3*2)+(2*0)+(1*8)=117
117 % 10 = 7
So 94042-08-7 is a valid CAS Registry Number.

94042-08-7SDS

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 dioxidanium,(1R,2R)-cyclohexane-1,2-diamine,platinum,dinitrate

1.2 Other means of identification

Product number -
Other names -

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:94042-08-7 SDS

94042-08-7Downstream Products

94042-08-7Relevant articles and documents

Novel platinum(II) complexes containing diaminocyclohexane and thiourea derivative ligands: Synthesis and X-ray crystal structure of (trans-1,2-diaminocyclohexane)dithioureaplatinum(II) nitrate monohydrate

Fang, Jing,Wei, Xin,Sapp, John B.,Deng, Yuanjian

, p. 5 - 10 (2014)

Six novel platinum(II) complexes of the form [Pt(dach)L2] (NO3)2, where dach = trans-1,2-diaminocyclohexane, L = thiourea (tu) or its derivatives, including 1-acetyl-2-thiourea, 1-ethyl-2-thiourea, 2-imidazolidinethione, 1,3-dimethyl-2-thiourea and 1,1,3,3-tetramethyl-2-thiourea, have been synthesized and characterized by elemental analysis, IR spectrometry, and NMR (1H and 13C) spectroscopy. The general synthetic procedure involves the reaction of [Pt(dach)(H2O)2](NO3)2, which is formed in situ by treating Pt(dach)I2 with silver nitrate, and two equivalents of tu or its derivatives. All the complexes are ionic compounds with nitrate counter ions and thus water soluble. The crystal structure of [Pt(dach)(tu)2](NO3)2·H2O is determined using a single crystal X-ray diffraction method. This compound crystallizes in the orthorhombic space group Pnma with centrosymmetry.

Process for the preparation of 1,2-diaminocyclohexane-platinum(II) complexes

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Page/Page column 2; 3, (2008/06/13)

A process for the preparation of diaminocyclohexane-platinum(II)-dicarboxylates has the following steps: B Conversion of K2PtX2 with 1,2-diaminocyclohexane (DACH) to (2): C Conversion of (2) with too little quantity of silver salt AgnA to (3): and removal of the resulting AgX precipitate. D Conversion of (3) with a dicarboxylate to (1): F Isolation of the product (1), wherein R1 and R2 together form a dicarboxylato group, X stands for Cl or I, A for a 1-2-valent anion of a mineral acid, and n stands for 1 or 2.

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