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173437-05-3

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173437-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173437-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,4,3 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 173437-05:
(8*1)+(7*7)+(6*3)+(5*4)+(4*3)+(3*7)+(2*0)+(1*5)=133
133 % 10 = 3
So 173437-05-3 is a valid CAS Registry Number.

173437-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethyl-2-(4-nitrophenyl)-3-phenylbutane

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:173437-05-3 SDS

173437-05-3Upstream product

173437-05-3Downstream Products

173437-05-3Relevant articles and documents

Preference of the mesolytic cleavage over the nuclear substitution observed in the ozone-mediated nitration of bicumene with nitrogen dioxide. Implication to the electron transfer nature of the Kyodai-nitration of arenes

Suzuki, Hitomi,Mori, Tadashi

, p. 647 - 648 (1996)

Ozone-mediated reaction of bicumene with nitrogen dioxide in dichloromethane at low temperature results in almost complete mesolytic cleavage of the hydrocarbon, accompanied by little or no nuclear nitration, in accordance with operation of the electron transfer process involving the nitrogen trioxide as initial electrophile.

Iron(III)-catalysed nitration of non-activated and moderately activated arenes with nitrogen dioxide-molecular oxygen under neutral conditions

Suzuki, Hitomi,Yonezawa, Shuji,Nonoyama, Nobuaki,Mori, Tadashi

, p. 2385 - 2389 (2007/10/03)

In the presence of molecular oxygen and a catalytic amount of tris(pentane-2,4-dionato)iron(III), non-activated and moderately activated arenes, which include alkylbenzenes, halogenobenzenes, phenolic ethers, naphthalene and derivatives, can be nitrated with nitrogen dioxide at ice-bath temperature or below to give the corresponding nitro derivatives in fair to good yields. An electron-transfer mechanism has been proposed, where an activated NO2-FeIII complex plays a key role in the cyclic process for converting arenes into nitroarenes.

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