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1033693-02-5

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1033693-02-5 Usage

Derivative

Methyl ester of 1H-Indole-3-carboxylic acid

Natural occurrence

Found in various plants

Uses

Flavoring agent in food, fragrance ingredient, precursor in synthesis of pharmaceuticals and agrochemicals

Potential role

Treatment of neurodegenerative diseases and cancer

Odor

Aromatic and fruity

Pesticide

Yes

Safety precautions

Handle with proper safety precautions due to potential health and environmental hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 1033693-02-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,3,6,9 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1033693-02:
(9*1)+(8*0)+(7*3)+(6*3)+(5*6)+(4*9)+(3*3)+(2*0)+(1*2)=125
125 % 10 = 5
So 1033693-02-5 is a valid CAS Registry Number.

1033693-02-5SDS

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 Propyl 1-methyl-1H-indole-3-carboxylate

1.2 Other means of identification

Product number -
Other names propyl 1-methylindole-3-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:1033693-02-5 SDS

1033693-02-5Downstream Products

1033693-02-5Relevant articles and documents

Regioselective Rh-catalyzed direct carbonylation of indoles to synthesize indole-3-carboxylates

Lang, Rui,Wu, Junliang,Shi, Lijun,Xia, Chungu,Li, Fuwei

supporting information; experimental part, p. 12553 - 12555 (2012/02/02)

Rh-catalyzed C-H carbonylation of indoles under 1 atm of CO has been achieved. Various substituted indoles and indole with free N-H could be carboxylated with linear- and/or cyclic-alcohol to give the desired indole-3-carboxylates with up to 92% yield. A mechanism involving Rh III initiated C-H metallation is proposed.

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