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94-85-9

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94-85-9 Usage

Chemical Properties

White or gray white crystals

Check Digit Verification of cas no

The CAS Registry Mumber 94-85-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94-85:
(4*9)+(3*4)+(2*8)+(1*5)=69
69 % 10 = 9
So 94-85-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO2/c1-3-12-8-5-6-10(13-4-2)9(11)7-8/h5-7H,3-4,11H2,1-2H3

94-85-9 Well-known Company Product Price

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  • Alfa Aesar

  • (L04296)  2,5-Diethoxyaniline, 96%   

  • 94-85-9

  • 1g

  • 188.0CNY

  • Detail
  • Alfa Aesar

  • (L04296)  2,5-Diethoxyaniline, 96%   

  • 94-85-9

  • 5g

  • 459.0CNY

  • Detail

94-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-Diethoxyaniline

1.2 Other means of identification

Product number -
Other names 2,4-DIFLUORO-5-NITROBENZENESULFONYL CHLORIDE

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:94-85-9 SDS

94-85-9Relevant articles and documents

A mild and selective Cu(II) salts-catalyzed reduction of nitro, azo, azoxy, N-aryl hydroxylamine, nitroso, acid halide, ester, and azide compounds using hydrogen surrogacy of sodium borohydride

Kalola, Anirudhdha G.,Prasad, Pratibha,Mokariya, Jaydeep A.,Patel, Manish P.

supporting information, p. 3565 - 3589 (2021/10/12)

The first mild, in situ, single-pot, high-yielding well-screened copper (II) salt-based catalyst system utilizing the hydrogen surrogacy of sodium borohydride for selective hydrogenation of a broad range of nitro substrates into the corresponding amine under habitancy of water or methanol like green solvents have been described. Moreover, this catalytic system can also activate various functional groups for hydride reduction within prompted time, with low catalyst-loading, without any requirement of high pressure or molecular hydrogen supply. Notably, this system explores a great potential to substitute expensive traditional hydrogenation methodologies and thus offers a greener and simple hydrogenative strategy in the field of organic synthesis.

Hydrazine-mediated reduction of nitro and azide functionalities catalyzed by highly active and reusable magnetic iron oxide nanocrystals

Cantillo, David,Moghaddam, Mojtaba Mirhosseini,Kappe, C. Oliver

, p. 4530 - 4542 (2013/06/05)

Iron oxide (Fe3O4) nanocrystals generated in situ from an inexpensive and readily available iron source catalyze the reduction of nitroarenes to anilines with unparalleled efficiency. The procedure is chemoselective, avoids the use of precious metals, and can be applied under mild reflux conditions (65 or 80 C) or using sealed vessel microwave heating in an elevated temperature regime (150 C). Utilizing microwave conditions, a variety of functionalized anilines have been prepared in nearly quantitative yields within 2-8 min at 150 C, in a procedure also successfully applied to the reduction of aliphatic nitro compounds and azides. The iron oxide nanoparticles are generated in a colloidal form, resulting in homogeneous solutions suitable for continuous flow processing. Selected examples of anilines of industrial importance have been prepared in a continuous regime using this protocol.

Reduction of Aromatic Nitro Compounds to Aromatic Amines by Sodium Trimethylsilanethiolate

Hwu, Jih Ru,Wong, Fung Fuh,Shiao, Min-Jen

, p. 5254 - 5255 (2007/10/02)

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