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

62134-47-8

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62134-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62134-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,3 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62134-47:
(7*6)+(6*2)+(5*1)+(4*3)+(3*4)+(2*4)+(1*7)=98
98 % 10 = 8
So 62134-47-8 is a valid CAS Registry Number.

62134-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-bromoanilino)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names Butanoic acid,4-[(2-bromophenyl)amino]-4-oxo

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:62134-47-8 SDS

62134-47-8Relevant academic research and scientific papers

N-Aryl Amides as Chemical Exchange Saturation Transfer Magnetic Resonance Imaging Contrast Agents

Cai, Xuekang,Zhang, Jia,Lu, Jiaqi,Yi, Long,Han, Zheng,Zhang, Shuixing,Yang, Xing,Liu, Guanshu

supporting information, p. 11705 - 11709 (2020/08/13)

Chemical exchange saturation transfer (CEST) MRI has recently emerged as a versatile molecular imaging approach in which diamagnetic compounds can be utilized to generate an MRI signal. To expand the scope of CEST MRI applications, herein, we systematical

Formation of Fused Tricyclic Azetidinones and Pyrrolidinones by Intramolecular SH2 Processes

Beckwith, A. L. J.,Boate, D. R.

, p. 4339 - 4348 (2007/10/02)

Treatment of a variety of suitably substituted sulfides of N-(o-halobenzyl)- or N-(o-halophenyl)azetidinone (e.g., 4 and 8) and -pyrrolidinone (e.g., 12 and 14) systems with either tributylstannane or tributyltin deuteride affords, by aryl radical substit

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