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35572-78-2

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35572-78-2 Usage

Definition

ChEBI: An amino-nitrotoluene that is 4,6-dinitrotoluene substituted at position 2 by an amino group.

Check Digit Verification of cas no

The CAS Registry Mumber 35572-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,7 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35572-78:
(7*3)+(6*5)+(5*5)+(4*7)+(3*2)+(2*7)+(1*8)=132
132 % 10 = 2
So 35572-78-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3O4/c1-4-6(8)2-5(9(11)12)3-7(4)10(13)14/h2-3H,8H2,1H3

35572-78-2 Well-known Company Product Price

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  • Supelco

  • (47749-U)  2-Amino-4,6-dinitrotoluenesolution  certified reference material, 1000 μg/mL in acetonitrile

  • 35572-78-2

  • 47749-U

  • 372.06CNY

  • Detail
  • Cerilliant

  • (ERA-017)  2-Amino-4,6-dinitrotoluene  vial of 100 mg, analytical standard

  • 35572-78-2

  • ERA-017-100MG

  • 1,023.75CNY

  • Detail

35572-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-4,6-dinitrotoluene

1.2 Other means of identification

Product number -
Other names 4-amino-2,6-dinitrotoluene

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:35572-78-2 SDS

35572-78-2Relevant articles and documents

ANALYTE DETECTION

-

, (2008/12/08)

The present invention relates to sensitive SE(R)RS based methods for detecting analytes such as explosives and drugs, which may be present in a sample at extremely low levels. The methods may be generally carried out in situ employing novel chemistry whic

Change in regioselectivity in the monoreduction of 2,4,6-trinitrotoluene with titanium(III) and vanadium(II) ions in the presence of iron(II) and copper(II) salts

Leibzon,Michalchenko,Leonova,Gultyai

, p. 1203 - 1207 (2007/10/03)

Small additives of iron(II) or copper(II) salts change the regioselectivity of 2,4,6-trinitrotoluene monoreduction with titanium(III) chloride affording predominantly less accessible 2-amino-4,6-dinitrotoluene over 4-amino-2,6-dinitrotoluene (from 25% when the reduction occurs in the absence of the iron and copper salts to 70% in the presence of these salts). A possible mechanism of the process is discussed.

The crystal structures of three primary products from the selective reduction of 2,4,6-trinitrotoluene

Graham, Duncan,Kennedy, Alan R.,McHugh, Callum J.,Smith, W. Ewen,David, William I. F.,Shankland, Kenneth,Shankland, Norman

, p. 161 - 165 (2007/10/03)

The crystal structures of three primary products from the selective reduction of 2,4,6-trinitrotoluene (TNT) have been determined by synchrotron X-ray powder diffraction (2-amino-4,6-dinitrotoluene) and single crystal X-ray diffraction (4-amino-2,6-dinitr

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