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5-(BENZYLOXY)-1H-INDOLE-2-CARBOHYDRAZIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20948-66-7

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20948-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20948-66-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,4 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20948-66:
(7*2)+(6*0)+(5*9)+(4*4)+(3*8)+(2*6)+(1*6)=117
117 % 10 = 7
So 20948-66-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H15N3O2/c17-19-16(20)15-9-12-8-13(6-7-14(12)18-15)21-10-11-4-2-1-3-5-11/h1-9,18H,10,17H2,(H,19,20)

20948-66-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenylmethoxy-1H-indole-2-carbohydrazide

1.2 Other means of identification

Product number -
Other names 5-(benzyloxy)-1H-indole-2-carbohydrazide

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:20948-66-7 SDS

20948-66-7Relevant academic research and scientific papers

Diversity-Oriented Synthesis of Calothrixins and Ellipticines

Dethe, Dattatraya H.,Murhade, Ganesh M.

, p. 6953 - 6962 (2016/02/19)

The divergent synthesis of calothrixins and ellipticines has been accomplished by utilising the one-pot formation of o-diacylarenes as a key intermediate through rearrangement of o-hydroxy ketone monoacyl hydrazones by lead tetraacetate mediated oxidation. The divergent synthesis of calothrixins and ellipticines has been accomplished by utilising the one-pot formation of o-diacylarenes as a key intermediate through rearrangement of o-hydroxy ketone monoacyl hydrazones by lead tetraacetate mediated oxidation.

Synthesis of Substituted 2-(1',3',4'-Oxadiazol-2'-yl)indoles

Sinnur, K. H.,Siddappa, S.,Hiremath, Shivayogi P.,Purohit, Muralidhar G.

, p. 716 - 720 (2007/10/02)

Substituted indole-2-carboxylic acid hydrazides (2) on refluxing with ethyl orthoformate give the respective 2-(1',3',4'-oxadiazol-2'-yl)indoles (4).These compounds have also been obtained by reacting 2 with formamide to get the corresponding N-formyl der

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