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1H-Indole-3-methanol, 1-[(3-chlorophenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92407-90-4

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92407-90-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92407-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,4,0 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92407-90:
(7*9)+(6*2)+(5*4)+(4*0)+(3*7)+(2*9)+(1*0)=134
134 % 10 = 4
So 92407-90-4 is a valid CAS Registry Number.

92407-90-4SDS

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 [1-[(3-chlorophenyl)methyl]indol-3-yl]methanol

1.2 Other means of identification

Product number -
Other names Oncrasin 72

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:92407-90-4 SDS

92407-90-4Downstream Products

92407-90-4Relevant academic research and scientific papers

Analogues and derivatives of oncrasin-1, a novel inhibitor of the C-terminal domain of RNA polymerase II and their antitumor activities

Wu, Shuhong,Wang, Li,Guo, Wei,Liu, Xiaoying,Liu, Jinsong,Wei, Xiaoli,Fang, Bingliang

experimental part, p. 2668 - 2679 (2011/06/27)

To optimize the antitumor activity of oncrasin-1, a small molecule RNA polymerase II inhibitor, we evaluated 69 oncrasin-1 analogues for their cytotoxic activity against normal human epithelial cells and K-Ras mutant tumor cells. About 40 of those compoun

Syntheses and in vitro antimycotic activities of 1-benzyl-3-(1-imidazolylmethyl)indoles

Cavrini,Gatti,Roveri,Cesaroni,Mazzoni,Fiorentini

, p. 662 - 668 (2007/10/02)

Syntheses of seventeen 1-benzyl-3-(1-imidazolylmethyl)indoles with substituents at the benzyl moiety and at the indole C-2 position are described. The compounds were tested for their antifungal activities in vitro determination of the minimum inhibitory concentration (MIC). Three compounds exhibited appreciable activities against Cr. neoformans.

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