Basic information

Product Name: 7-AMino-5-broMoindole-2-carboxylic acid ethyl ester
Synonyms: 7-AMino-5-broMoindole-2-carboxylic acid ethyl ester
CAS NO:91119-16-3
Molecular Formula: C11H11BrN2O2
Molecular Weight: 283.12124
EINECS: N/A
Product Categories: N/A
Mol File: 91119-16-3.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 7-AMino-5-broMoindole-2-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 7-AMino-5-broMoindole-2-carboxylic acid ethyl ester(91119-16-3)
EPA Substance Registry System: 7-AMino-5-broMoindole-2-carboxylic acid ethyl ester(91119-16-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 91119-16-3(Hazardous Substances Data)

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91119-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91119-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,1,1 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91119-16:
(7*9)+(6*1)+(5*1)+(4*1)+(3*9)+(2*1)+(1*6)=113
113 % 10 = 3
So 91119-16-3 is a valid CAS Registry Number.

91119-16-3SDS

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	ethyl 7-amino-5-bromo-1H-indole-2-carboxylate

1.2 Other means of identification

Product number	-
Other names	7-AMINO-5-BROMOINDOLE-2-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:91119-16-3 SDS

91119-16-3Upstream product

91119-28-7 7-nitro-5-bromo-1H-indole-2-carboxylic acid ethyl ester

91119-16-3Downstream Products

91119-16-3Relevant academic research and scientific papers

Synthesis of Isomeric Benzodipyrroles

Katti, H. A.,Siddappa, S.

, p. 1205 - 1208 (2007/10/02)

Ethyl aminoindole-2-carboxylates (2), obtained by catalytic reduction of ethyl nitroindole-2-carboxylates (1) using Raney nickel, when subjected to Japp-Klingemann reaction furnish the respective indolylhydrazones (3).The latter undergo cyclization with H2SO4 to yield different isomeric benzodipyrroles (4-6).

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