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28202-30-4

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28202-30-4 Usage

General Description

2-Tetrafluoroethoxy-5-nitrotoluene is a chemical compound with the molecular formula C8H6F4NO3. It is a nitro compound with a molecular weight of 231.13 g/mol. This chemical is used in the synthesis of pharmaceuticals and agrochemicals. It is a pale yellow solid at room temperature and is insoluble in water. 2-Tetrafluoroethoxy-5-nitrotoluene is also used as an intermediate in the production of dyes and pigments. It is important to handle this chemical with care, as it can be harmful if inhaled, swallowed, or comes into contact with skin.

Check Digit Verification of cas no

The CAS Registry Mumber 28202-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,0 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28202-30:
(7*2)+(6*8)+(5*2)+(4*0)+(3*2)+(2*3)+(1*0)=84
84 % 10 = 4
So 28202-30-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F4NO3/c1-5-4-6(14(15)16)2-3-7(5)17-9(12,13)8(10)11/h2-4,8H,1H3

28202-30-4SDS

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-methyl-4-nitro-1-(1,1,2,2-tetrafluoroethoxy)benzene

1.2 Other means of identification

Product number -
Other names EINECS 248-896-4

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:28202-30-4 SDS

28202-30-4Upstream product

28202-30-4Relevant articles and documents

Urea derivatives and their use as herbicides

-

, (2008/06/13)

Compounds, useful as herbicides, of the formula SPC1 Wherein R1 is haloalkyl, halocycloalkyl, haloalkenyl, or halocycloalkenyl; n1 is 1 or 2; R4 is halogen, trifluoromethyl, alkyl, or alkoxy; n2 is 0, 1, 2, or 3; R2 is hydrogen or alkyl; and R3 is alkyl or alkoxy. Methods for making these compounds.

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