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2-chloro-1-(2-chlorobenzyl)-3-[(E)-2-nitroethenyl]-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77655-62-0

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77655-62-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77655-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,5 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77655-62:
(7*7)+(6*7)+(5*6)+(4*5)+(3*5)+(2*6)+(1*2)=170
170 % 10 = 0
So 77655-62-0 is a valid CAS Registry Number.

77655-62-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-[(2-chlorophenyl)methyl]-3-[(E)-2-nitroethenyl]indole

1.2 Other means of identification

Product number -
Other names -

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:77655-62-0 SDS

77655-62-0Downstream Products

77655-62-0Relevant academic research and scientific papers

SINTESI ED ATTIVITA ANTIBATTERICA IN VITRO DI N-METILNITRONI E NITROVINILI DERIVATI DA ALCUNE 2-CLOROINDOL-3-CARBOSSIALDEIDI N-SOSTITUITE

Gatti, R.,Cavrini, V.,Roveri, P.,Bianucci, F.,Legnani, P.

, p. 102 - 108 (2007/10/02)

N-methylnitrones and nitrovinyl derivatives from 1-substituted-2-chloroindole-3-carboxaldehydes were synthesized and evaluated for their in vitro antibacterial activity.Some nitrovinyl derivatives displayed good in vitro activity against Gram-positive bacteria; the compound (II e), 1-(o-chlorobenzyl)-2-chloro-3-(2-nitroethenyl)indole, was more active than nitrofurantoin against Staphylococcus aureus and Streptococcus pyogenes.Some structure-activity relationships are discussed.

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