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10075-49-7

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10075-49-7 Usage

General Description

5-Bromo-1,3-dimethyl-1H-indole is a chemical compound with the molecular formula C10H10BrN. It is a derivative of indole, which is a widely occurring compound in nature and a key component of many pharmaceutical drugs and natural products. The presence of a bromine atom and two methyl groups on the indole ring gives this compound unique chemical and biological properties. 5-Bromo-1,3-dimethyl-1H-indole is used as a building block in the synthesis of various pharmaceuticals and agrochemicals, and it also has potential applications in the field of materials science and organic electronics. Its structural diversity and reactivity make it a valuable compound for the development of new drugs and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 10075-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,7 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10075-49:
(7*1)+(6*0)+(5*0)+(4*7)+(3*5)+(2*4)+(1*9)=67
67 % 10 = 7
So 10075-49-7 is a valid CAS Registry Number.

10075-49-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-3-methyl-5-bromoindole

1.2 Other means of identification

Product number -
Other names 5-bromo-1,3-dimethyl-1H-indole

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:10075-49-7 SDS

10075-49-7Downstream Products

10075-49-7Relevant articles and documents

Enantioselective synthesis of pyrroloindolines by a formal [3 + 2] cycloaddition reaction

Repka, Lindsay M.,Ni, Jane,Reisman, Sarah E.

, p. 14418 - 14420 (2010)

(R)-BINOL?SnCl4 was found to catalyze a formal [3 + 2] cycloaddition reaction between C(3)-substituted indoles and 2-amidoacrylates to provide pyrroloindolines. A variety of pyrroloindolines were prepared with high enantioselectivity in one step from simple precursors. This methodology is expected to facilitate the total synthesis of pyrroloindoline alkaloids, an important class of biologically active natural products.

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Noland,W.E.,Reich,C.

, p. 828 - 832 (1967)

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SELECTIVE INHIBITORS OF CLINICALLY IMPORTANT MUTANTS OF THE EGFR TYROSINE KINASE

-

, (2019/01/21)

The present invention provides compounds of Formula (I) or a subgeneric structure or species thereof, or a pharmaceutically acceptable salt, ester, solvate, and/or prodrug thereof, and methods and compositions for treating or ameliorating abnormal cell pr

SUBSTITUTED QUINOXALINE DERIVATIVES

-

Page/Page column 292, (2016/12/01)

The present invention relates to substituted quinoxaline derivatives. These compounds are useful for the prevention and/or treatment of several medical conditions including hyperproliferative disorders and diseases.

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