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4(3H)-Quinazolinone, 3-[2-(2-bromo-1H-indol-3-yl)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

807354-69-4

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807354-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 807354-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,7,3,5 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 807354-69:
(8*8)+(7*0)+(6*7)+(5*3)+(4*5)+(3*4)+(2*6)+(1*9)=174
174 % 10 = 4
So 807354-69-4 is a valid CAS Registry Number.

807354-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[2-(2-bromo-1H-indol-3-yl)ethyl]quinazolin-4-one

1.2 Other means of identification

Product number -
Other names 3-[2-(2-bromoindol-3-yl)ethyl]-4(3H)-quinazolinone

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:807354-69-4 SDS

807354-69-4Relevant academic research and scientific papers

Concise synthesis of quinazoline alkaloids, luotonins A and B, and rutaecarpine

Harayama, Takashi,Hori, Akihiro,Serban, Georgeta,Morikami, Yoshiaki,Matsumoto, Takuya,Abe, Hitoshi,Takeuchi, Yasuo

, p. 10645 - 10649 (2007/10/03)

The total synthesis of luotonin A was achieved in excellent yield by using a Pd-assisted biaryl coupling reaction of N-(bromoquinolinyl)methylquinazolinone with Cy3P and KOAc. The successive treatment of luotonin A with NBS and aq. AgNO3 gave luotonin B in good yield. Although the Pd-assisted coupling reaction of N-(2-bromoindolyl)ethylquinazolinone with Cy3P and KOAc yielded rutaecarpine in poor yield, N-acetate under the same reaction conditions yielded the desired rutaecarpine directly in excellent yield. Graphical Abstract.

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