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7-bromo-6-methoxy-2-methylquinoline-5,8-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61895-37-2

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61895-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61895-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,9 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61895-37:
(7*6)+(6*1)+(5*8)+(4*9)+(3*5)+(2*3)+(1*7)=152
152 % 10 = 2
So 61895-37-2 is a valid CAS Registry Number.

61895-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-bromo-6-methoxy-2-methylquinoline-5,8-dione

1.2 Other means of identification

Product number -
Other names 7-Brom-6-methoxy-2-methyl-5,8-chinolindion

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:61895-37-2 SDS

61895-37-2Downstream Products

61895-37-2Relevant academic research and scientific papers

Lavendamycin analogues and methods of synthesizing and using lavendamycin analogues

-

Page/Page column 12, (2010/10/20)

Lavendamycin analogues, methods for their synthesis, and methods for their use in the treatment of diseases such as cancer and HIV infection are described.

Total Synthesis of Novel 6-Substituted Lavendamycin Antitumor Agents

Seradj, Hassan,Cai, Wen,Erasga, Noe O.,Chenault, Darrell V.,Knuckles, Kathryn A.,Ragains, Justin R.,Behforouz, Mohammad

, p. 473 - 476 (2007/10/03)

(Equation presented) Novel 6-substituted lavendamycins have been synthesized for the first time. The key step in these syntheses is a Pictet-Spengler condensation (Scheme 1). Efficient methods for the synthesis of each compound, including a novel reaction for the facile introduction of alkylamino groups at the C-6 position of the lavendamycin system, are discussed. Possible mechanisms for these reactions are also presented.

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