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177200-90-7

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177200-90-7 Usage

Molecular class

chemical compound

Compound class

indole

Structure

derivative of indole-1,3-dicarboxylic acid with a tert-butyl and ethyl ester group attached to the 1 and 3 positions, respectively

Usage

building block for the synthesis of various indole derivatives and pharmaceutical compounds in organic synthesis and medicinal chemistry

Importance

unique structure and reactivity make it an important intermediate for the production of complex organic molecules with potential biological activity.

Check Digit Verification of cas no

The CAS Registry Mumber 177200-90-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,2,0 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 177200-90:
(8*1)+(7*7)+(6*7)+(5*2)+(4*0)+(3*0)+(2*9)+(1*0)=127
127 % 10 = 7
So 177200-90-7 is a valid CAS Registry Number.

177200-90-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-(tert-butoxycarbonyl)indole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 1H-INDOLE-1,3-DICARBOXYLIC ACID, 1-(1,1-DIMETHYLETHYL)3-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:177200-90-7 SDS

177200-90-7Downstream Products

177200-90-7Relevant articles and documents

2,9-DIAMINO- AND 2-AMINO-8-CARBAMOYL-4-HYDROXY-ALKANOIC ACID AMIDE DERIVATIVES

-

, (2008/06/13)

Compounds of the formula I STR1 in which R 1 is arylamino, N-aryl-N-(lower alkoxy-lower alkyl)-amino, N-aryl-N-aryl-lower alkyl-amino or heterocyclyl bonded via a ring carbon atom, X is a carbonyl or methylene group, R 2 and R 3 independently of one another are hydrogen or lower alkyl or, together with the carbon atom with which they are bonded, are a cycloalkylidene radical, R 4 is hydrogen, lower alkyl, lower alkanoyl or lower alkoxycarbonyl, R 5 is hydroxyl, lower alkanoyloxy or lower alkoxycarbonyloxy, R 6 is hydrogen, lower alkyl, lower alkenyl, lower alkynyl, cycloalkyl, cycloalkyl-lower alkyl, aryl-lower alkyl or heteroaryl-lower alkyl having 5 to 7 ring atoms in the heteroaryl ring and R 7 is hydrogen or lower alkyl, or R 6 and R. sub.7, together with the carbon atom with which they are bonded, are a cydoalkylidene radical and R 8 denotes an aliphatic, cycloaliphatic-aliphatic or heteroarylaliphatic radical, and their salts can be used as active ingredients for medicaments for treatment of high blood pressure.

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