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1226762-74-8

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1226762-74-8 Usage

General Description

Ethyl 7-bromoquinoline-3-carboxylate is a chemical compound with the molecular formula C14H11BrNO2. It is a yellow crystalline powder that is often used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Ethyl 7-broMoquinoline-3-carboxylate contains a bromine atom, a quinoline ring, and an ethyl ester group, and it is a derivative of quinoline, which is a heterocyclic aromatic compound. Ethyl 7-bromoquinoline-3-carboxylate has various applications in the field of organic chemistry and chemical research, and it is utilized as a building block for the preparation of other chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1226762-74-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,6,7,6 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1226762-74:
(9*1)+(8*2)+(7*2)+(6*6)+(5*7)+(4*6)+(3*2)+(2*7)+(1*4)=158
158 % 10 = 8
So 1226762-74-8 is a valid CAS Registry Number.

1226762-74-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 7-bromoquinoline-3-carboxylate

1.2 Other means of identification

Product number -
Other names 7-bromoquinoline-3-carboxylic acid ethyl ester

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:1226762-74-8 SDS

1226762-74-8Relevant articles and documents

Selective reductive annulation reaction for direct synthesis of functionalized quinolines by a cobalt nanocatalyst

Xie, Rong,Lu, Guang-Peng,Jiang, Huan-Feng,Zhang, Min

, p. 239 - 243 (2020/02/15)

Due to the extensive applications of quinolines, the search for selective construction of such products has long been an attractive subject in scientific community. Herein, by developing a new N-doped ZrO2@C supported cobalt nanomaterial, it has been successfully applied as an efficient catalyst for the reductive annulation of 2-nitroaryl carbonyls with alkynoates and alkynones. The catalytic transformation allows synthesizing a wide array of funcitonalized quinolines with the merits of broad substrate scope, good functional group tolerance, excellent hydrogen transfer selectivity, reusable earth-abundant metal catalyst, and operational simplicity. The developed chemistry paves the ways for further design of hydrogen transfer-mediated coupling reactions by developing heterogeneous catalysts with suitable supports.

OXADIAZOLE INHIBITORS OF HIPK2 FOR TREATING KIDNEY FIBROSIS

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Paragraph 0051, (2018/07/31)

Compounds that are selective inhibitors of Smad3 activation are disclosed. The compounds have the structure (I) in which Z is an oxadiazole. The compounds disclosed are useful in treatment of fibrotic disease, particularly renal fibrosis, and similar dise

FATTY ACID SYNTHASE INHIBITORS

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Page/Page column 58; 59, (2014/01/07)

Disclosed are compounds having Formula (I), wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, Y, m, and n are defined herein and methods of using the same.

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