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Acetamide, N-(2-bromo-5-ethoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139085-94-2

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139085-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139085-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,0,8 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 139085-94:
(8*1)+(7*3)+(6*9)+(5*0)+(4*8)+(3*5)+(2*9)+(1*4)=152
152 % 10 = 2
So 139085-94-2 is a valid CAS Registry Number.

139085-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-bromo-5-ethoxyphenyl)acetamide

1.2 Other means of identification

Product number -
Other names Acetamide,N-(2-bromo-5-ethoxyphenyl)

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:139085-94-2 SDS

139085-94-2Upstream product

139085-94-2Downstream Products

139085-94-2Relevant academic research and scientific papers

Mild C - H halogenation of anilides and the isolation of an unusual palladium(I)-palladium(II) species

Bedford, Robin B.,Haddow, Mairi F.,Mitchell, Charlotte J.,Webster, Ruth L.

, p. 5524 - 5527 (2011)

Reducing the load: A facile palladium-catalyzed ortho-selective bromination and chlorination of anilides occurs under aerobic conditions at room temperature when N-halosuccinimides (NXS) are used in the presence of p-toluenesulfonic acid (PTSA). The orthopalladated PTSA complex is not only catalytically competent but also undergoes a reductive process to yield an unusual PdI-PdII tetramer (see structure; Pdgreen, Ored, Syellow, Cgray). Copyright

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