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2-Butenoic acid, 4-[(2-acetylphenyl)amino]-4-oxo-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86162-55-2

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86162-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86162-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,6 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 86162-55:
(7*8)+(6*6)+(5*1)+(4*6)+(3*2)+(2*5)+(1*5)=142
142 % 10 = 2
So 86162-55-2 is a valid CAS Registry Number.

86162-55-2SDS

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 4-(2-acetylanilino)-4-oxobut-2-enoic acid

1.2 Other means of identification

Product number -
Other names 2-Butenoic acid,4-[(2-acetylphenyl)amino]-4-oxo-,(Z)

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:86162-55-2 SDS

86162-55-2Downstream Products

86162-55-2Relevant academic research and scientific papers

Novel Approach to Pyrroloquinoline-1,5-diones

AlKhathlan, Hamad Z.

, p. 1984 - 1996 (2007/10/02)

The condensation of 2-aminoacetophenone with acid anhydrides is investigated.Different fused 4-quinolone derivatives were prepared in one step via this condensation.In addition different N-substituted imides were also obtained.

Ortho Substituent Effects in Amide Hydrolysis of Maleanilic Acid Derivatives. Stabilization of Positive Charge Developed in the Transition State

Suh, Junghun,Kim, Mahn Joo,Kim, Chong Bok

, p. 2453 - 2456 (2007/10/02)

The effects of ortho substituents on the rate of the hydrolysis of maleanilic acid derivatives have been studied.The rate is enhanced up to 55 times by polar substituents, while it is retarded greatly by nonpolar substituents.The acceleration by the polar

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