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676448-17-2

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676448-17-2 Usage

General Description

4-Bromoindole-1-carboxylic Acid Tert-Butyl Ester is a specialized chemical compound that combines indole and tert-butyl ester. The term "4-Bromo" suggests its bromine-substituted, specifically positioned at the fourth carbon in the indole structure. Indole is a heterocyclic aromatic compound, which is the parent structure of many natural substances. Carboxylic acid refers to the presence of a carboxyl functional group, while the Tert-butyl ester refers to an ester derivative with a tertiary butyl group. This chemical compound has specific applications in the field of biochemical research, and it is commonly used as an intermediate in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 676448-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,4,4 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 676448-17:
(8*6)+(7*7)+(6*6)+(5*4)+(4*4)+(3*8)+(2*1)+(1*7)=202
202 % 10 = 2
So 676448-17-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H13BrN2O2/c1-12(2,3)17-11(16)15-10-6-4-5-9(13)8(10)7-14-15/h4-7H,1-3H3

676448-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-BOC-4-Bromoindole

1.2 Other means of identification

Product number -
Other names tert-butyl 4-bromoindole-1-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:676448-17-2 SDS

676448-17-2Relevant articles and documents

Rhodium(II)-Catalyzed [4+3] Cyclization of Triazoles with Indole Derivatives and Its Application in the Total Synthesis of (±)-Aurantioclavine

Duan, Shengguo,Xue, Bing,Meng, Hui,Ye, Zihang,Xu, Ze-Feng,Li, Chuan-Ying

supporting information, p. 1145 - 1152 (2021/04/26)

An efficient rhodium(II)-catalyzed [4+3] cyclization reaction of 1-sulfonyl-1,2-3-triazoles and indoles was developed. Azepino[5,4,3- cd]indoles, which are widely distributed in ergot alkaloids with various biological activities, could be obtained in good

Substituted olefin compound, and preparation method and application thereof

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Paragraph 0233; 0234; 0235; 0236, (2018/05/16)

The invention provides a substituted olefin compound, and a preparation method and application thereof. Specifically, the application provides a substituted olefin compound, a stereoisomer, prodrug, solvate, and pharmaceutically acceptable salt or ester of the substituted olefin compound, a preparation method of the substituted olefin compound, and an application in preparing medicines for treating diseases relative to an excessive activity of estrogen receptors (such as ERalpha).

3-(1H-INDOL-2-YL)-1H-INDAZOLES AND THERAPEUTIC USES THEREOF

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Paragraph 0694; 0695, (2017/02/28)

Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of an indazole compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., cancer, abnormal cellular proliferation, angiogenesis, fibrotic disorders, bone or cartilage diseases, and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as genetic diseases and neurological conditions/disorders/diseases due to mutations or dysregulation of the Wnt pathway and/or of one or more of Wnt signaling components. Also provided are methods for treating Wnt-related disease states.

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