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786704-07-2

2-Bromo-1-methyl-1H-indole-3-acetic acid ethyl ester is a chemical compound that belongs to the ester class. It is a derivative of 2-Bromoindole, which has potential antineoplastic properties. This versatile compound is utilized in various fields, including pharmaceuticals, plant biology research, and antimicrobial studies.
Used in Pharmaceutical Industry:
2-Bromo-1-methyl-1H-indole-3-acetic acid ethyl ester is used as a synthetic intermediate for the development of various indole derivatives. These derivatives have potential applications in the treatment of various diseases and disorders.
Used in Plant Biology Research:
In plant biology, 2-Bromo-1-methyl-1H-indole-3-acetic acid ethyl ester is used as a tool to study the growth and development of plant tissues. Its ability to modify these processes aids researchers in understanding the underlying mechanisms and developing strategies for crop improvement.
Used in Antimicrobial Applications:
2-Bromo-1-methyl-1H-indole-3-acetic acid ethyl ester is also being studied for its potential antimicrobial and antifungal properties. This makes it a promising candidate for the development of new drugs to combat resistant infections and control the spread of various pathogens.

786704-07-2

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786704-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 786704-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,6,7,0 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 786704-07:
(8*7)+(7*8)+(6*6)+(5*7)+(4*0)+(3*4)+(2*0)+(1*7)=202
202 % 10 = 2
So 786704-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H14BrNO2/c1-3-17-12(16)8-10-9-6-4-5-7-11(9)15(2)13(10)14/h4-7H,3,8H2,1-2H3

786704-07-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(2-bromo-1-methylindol-3-yl)acetate

1.2 Other means of identification

Product number -
Other names (2-bromo-1-methyl-1H-indol-3-yl)acetic 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:786704-07-2 SDS

786704-07-2Downstream Products

786704-07-2Relevant articles and documents

Cycloaddition chemistry of 2-vinyl-substituted indoles and related heteroaromatic systems

Padwa, Albert,Lynch, Stephen M.,Mejia-Oneto, Jose M.,Zhang, Hongjun

, p. 2206 - 2218 (2007/10/03)

(Chemical Equation Presented) The intramolecular Diels-Alder cycloaddition reaction (IMDAF) of several N-phenylsulfonylindolyl-substituted furanyl carbamates containing a tethered π-bond on the indole ring were examined as an approach to the iboga alkaloi

Intramolecular [3 + 2]-cycloaddition reaction of push-pull dipoles across heteroaromatic π-systems

Mejia-Oneto, Jose M.,Padwa, Albert

, p. 3241 - 3244 (2007/10/03)

(Chemical Equation Presented) Push-pull dipoles generated from the Rh(II)-catalyzed reaction of diazo imides containing tethered heteroaromatic rings undergo successful [3 + 2]-cycloaddition across the 2,3-π-bond to provide novel pentacyclic compounds in

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