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2-Quinolinecarboxylic acid, pentafluorophenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

148315-27-9

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148315-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148315-27-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,3,1 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 148315-27:
(8*1)+(7*4)+(6*8)+(5*3)+(4*1)+(3*5)+(2*2)+(1*7)=129
129 % 10 = 9
So 148315-27-9 is a valid CAS Registry Number.

148315-27-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3,4,5,6-pentafluorophenyl) quinoline-2-carboxylate

1.2 Other means of identification

Product number -
Other names perfluorophenyl quiline-2-carboxylate

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:148315-27-9 SDS

148315-27-9Relevant academic research and scientific papers

Aminolysis of aryl ester using tertiary amine as amino donor via c-o and c-n bond activations

Bao, Yong-Sheng,Zhaorigetu, Bao,Agula, Bao,Baiyin, Menghe,Jia, Meilin

, p. 803 - 808 (2014/04/03)

An aminolysis reaction between various aryl esters and inert tertiary amines by C-O and C-N bond activations has been developed for the selective synthesis of a broad scope of tertiary amides under neutral and mild conditions. The mechanism may undergo the two key steps of oxidative addition of acyl C-O bond in parent ester and C-N bond cleavage of tertiary amine via an iminium-type intermediate.

Transesterification for synthesis of carboxylates using aldehydes as acyl donors via C-H and C-O bond activations

Bao, Yong-Sheng,Chen, Chao-Yue,Huang, Zhi-Zhen

, p. 8344 - 8349,6 (2020/10/15)

A new type of transesterification between aryl, heteroaryl, alkyl N-heteroarene-2-carboxylates and various aldehydes by C-H and C-O bond activations has been developed for the synthesis of versatile carboxylates. A possible mechanism containing oxidative addition of acyl-O bond in parent ester and radical cleavage of sp2 C-H bond in aldehyde is proposed.

Ramoplanin derivatives possessing antibacterial activity

-

Page/Page column 38; 62, (2010/11/23)

Novel ramoplanin derivatives are disclosed. These ramoplanin derivatives exhibit antibacterial activity. As the compounds of the subject invention exhibit potent activities against gram positive bacteria, they are useful antimicrobial agents. Methods of synthesis and of use of the compounds are also disclosed.

Synthesis and Biological Properties of Pyrimidine 2'-Deoxynucleosides Modified with Quinaldic Acid

Ektova, L.V.,Yartseva, I.V.,Khorosheva, E.V.,Ivanova, T.P.,Yavorskaya, N.P.,Melnik, S.Ya.

, p. 540 - 546 (2007/10/02)

O-Quinaldoyl derivatives of thymidine, 2'-deoxyuridine, and 5-trimethylsilyl-2'-deoxyuridine were synthesized. 5'-Deoxy-5'-(quinoline-2-carbonylamino)- and 5'-deoxy-5'-thymidine were obtained by the reaction of 5'

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