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1033265-55-2

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1033265-55-2 Usage

General Description

Tert-butyl 5-Methoxyindole-3-carboxylate is a chemical compound with the molecular formula C16H33NO3. It is a derivative of indole, a heterocyclic aromatic organic compound, and is commonly used in organic synthesis and pharmaceutical research. The presence of a tert-butyl group in the structure increases the compound's stability and makes it more resistant to chemical reactions. The 5-methoxy and 3-carboxylate groups provide additional functional groups for potential chemical modifications. Tert-butyl 5-Methoxyindole-3-carboxylate may be used in the development of new drugs and pharmaceuticals due to its unique structure and potential biological activity.

Check Digit Verification of cas no

The CAS Registry Mumber 1033265-55-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,3,2,6 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1033265-55:
(9*1)+(8*0)+(7*3)+(6*3)+(5*2)+(4*6)+(3*5)+(2*5)+(1*5)=112
112 % 10 = 2
So 1033265-55-2 is a valid CAS Registry Number.

1033265-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl 5-methoxy-1H-indole-3-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 5-methoxy-1H-indole-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:1033265-55-2 SDS

1033265-55-2Downstream Products

1033265-55-2Relevant articles and documents

Palladium-catalyzed synthesis of 3-indolecarboxylic acid derivatives

Soederberg, Bjoern C. G.,Banini, Serge R.,Turner, Michael R.,Minter, Aaron R.,Arrington, Amanda K.

, p. 903 - 912 (2008/09/21)

Indoles having an ester functionality in the 3-position were prepared from 2-(2-nitrophenyl)propenoic acid derivatives via a palladium-catalyzed reductive N-heteroannulation using carbon monoxide as the ultimate reducing agent. The starting materials were

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