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446-33-3

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446-33-3 Usage

Chemical Properties

colorless to light yellow liqui

Check Digit Verification of cas no

The CAS Registry Mumber 446-33-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,4 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 446-33:
(5*4)+(4*4)+(3*6)+(2*3)+(1*3)=63
63 % 10 = 3
So 446-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6FNO2/c1-5-4-6(8)2-3-7(5)9(10)11/h2-4H,1H3

446-33-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Alfa Aesar

  • (A13944)  5-Fluoro-2-nitrotoluene, 98+%   

  • 446-33-3

  • 10g

  • 701.0CNY

  • Detail
  • Alfa Aesar

  • (A13944)  5-Fluoro-2-nitrotoluene, 98+%   

  • 446-33-3

  • 50g

  • 935.0CNY

  • Detail
  • Aldrich

  • (F12405)  5-Fluoro-2-nitrotoluene  97%

  • 446-33-3

  • F12405-10G

  • 452.79CNY

  • Detail
  • Aldrich

  • (F12405)  5-Fluoro-2-nitrotoluene  97%

  • 446-33-3

  • F12405-50G

  • 908.74CNY

  • Detail

446-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Fluoro-2-nitrotoluene

1.2 Other means of identification

Product number -
Other names Fluoronitrotoluene5

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:446-33-3 SDS

446-33-3Relevant articles and documents

Preparation method of 2- bromo -4- fluoro -6- methyl phenol (by machine translation)

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Paragraph 0015; 0023, (2020/03/17)

2 - (,) The process for preparing .2 -methylnitrobenzene, (:) by subjecting 1 fluorine - 2 2-methylnitrobenzene prepared in step (:) to a reduction reaction 4 - to prepare; fluorine - 2 2-methylphenol. 2. The method comprises the following steps :) of nitrosation reaction 1 (4 -) diazo hydrolysis. 4 - g - 2 2-methylphenol prepared by the following steps: The process of the present invention, is simple 3% by diazotization reaction: to prepare 3 the 2 fluorine - 2 2-methylphenol obtained in step (4 -) by means of a reduction reaction step (4 -) to form 4 - fluorine. 2 2 (4 2 -)-methylphenol prepared by the same step as a process. for the preparation of fine chemical products by 2 - means of the bromination reaction step of the preparation, method as shown in the following step (. a).]) The method comprises the following steps: (a)) diazo reaction : (by machine translation)

Bicyclic And Tricyclic Compounds As KAT II Inhibitors

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Page/Page column 26-27, (2010/12/31)

Compounds of Formula X: wherein A, X, Y, Z, R5, R6a, and R6b are as defined herein, and pharmaceutically acceptable salts thereof, are described as useful for the treatment of cognitive deficits associated with schizophrenia and other neurodegenerative and/or neurological disorders in mammals, including humans.

Bis(dealkoxycarbonylation) of nitroarylmalonates: A facile entry to alkylated nitroaromatics

Gurjar,Reddy,Murugaiah,Murugaiah

, p. 1659 - 1661 (2007/10/03)

A simple approach to alkylated nitroaromatics from substituted nitroaryl malonic esters by double decarboxylation is detailed.

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