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146117-78-4

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146117-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146117-78-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,1,1 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 146117-78:
(8*1)+(7*4)+(6*6)+(5*1)+(4*1)+(3*7)+(2*7)+(1*8)=124
124 % 10 = 4
So 146117-78-4 is a valid CAS Registry Number.

146117-78-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4aS,10bS)-8-chloro-4-methyl-1,2,4a,5,6,10b-hexahydrobenzo[f]quinolin-3-one

1.2 Other means of identification

Product number -
Other names 8-Chloro-4-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo(f)quinolin-3(2H)-one

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:146117-78-4 SDS

146117-78-4Downstream Products

146117-78-4Relevant articles and documents

Resolution of δ-lactams provides access to nonracemic benzoquinolinones: The synthesis of LY300502 and LY300503

Astleford, Bret A.,Audia, James E.,Deeter, Jack,Heath, Perry C.,Janisse, Samantha K.,Kress, Thomas J.,Wepsiec, James P.,Weigel, Leland O.

, p. 4450 - 4454 (1996)

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Method of preventing prostatic cancer development

-

, (2008/06/13)

A series of benzoquinolin-3-ones are pharmaceuticals effective in preventing the development of prostatic cancer, or preventing or treating the metastasis to bone of prostatic cancer.

Process for preparation of benzo[f]quinolinones

-

, (2008/06/13)

A series of benzoquinolin-3-ones are pharmaceuticals effective in treating conditions consequent on both Type I and Type II 5α-reductase and their preparation is disclosed.

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