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112515-42-1

112515-42-1

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112515-42-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112515-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,5,1 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112515-42:
(8*1)+(7*1)+(6*2)+(5*5)+(4*1)+(3*5)+(2*4)+(1*2)=81
81 % 10 = 1
So 112515-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H14N4O/c25-19(15-10-22-17-8-4-2-6-13(15)17)20-23-11-18(24-20)14-9-21-16-7-3-1-5-12(14)16/h1-11,21-22H,(H,23,24)

112515-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-indol-3-yl-[5-(1H-indol-3-yl)-1H-imidazol-2-yl]methanone

1.2 Other means of identification

Product number -
Other names topsentin A

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:112515-42-1 SDS

112515-42-1Downstream Products

112515-42-1Relevant articles and documents

Topsentin, Bromotopsentin, and Dihydrodeoxybromotopsentin: Antiviral and Antitumor Bis(indolyl)imidazoles from Caribbean Deep-Sea Sponges of the Family Halichondriidae Structural and Synthetic Studies

Tsujii, Shinji,Rinehart, Kenneth L.,Gunasekera, Sarath P.,Kashman, Yoel,Cross, Susan S.,et al.

, p. 5446 - 5453 (2007/10/02)

Isolation and structure elucidation of topsentin (1) and bromotopsentin (2) are described.These novel indole alkaloids have been shown to have antitumor and antiviral activities.Their structures were determined on the basis of spectral data, and bromotopsentin was correlated structurally with topsentin by catalytic debromination.Syntheses of 1 and several analogues are also reported.

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