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866211-50-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 866211-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,2,1 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 866211-50:
(8*8)+(7*6)+(6*6)+(5*2)+(4*1)+(3*1)+(2*5)+(1*0)=169
169 % 10 = 9
So 866211-50-9 is a valid CAS Registry Number.

866211-50-9SDS

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 4-fluoro-3,3-dimethyl-1H-indol-2-one

1.2 Other means of identification

Product number -
Other names 2H-Indol-2-one,4-fluoro-1,3-dihydro-3,3-dimethyl

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:866211-50-9 SDS

866211-50-9Relevant articles and documents

Design and synthesis of a novel 2-oxindole scaffold as a highly potent and brain-penetrant phosphodiesterase 10A inhibitor

Yoshikawa, Masato,Kamisaki, Haruhi,Kunitomo, Jun,Oki, Hideyuki,Kokubo, Hironori,Suzuki, Akihiro,Ikemoto, Tomomi,Nakashima, Kosuke,Kamiguchi, Naomi,Harada, Akina,Kimura, Haruhide,Taniguchi, Takahiko

, p. 7138 - 7149 (2015/11/16)

Highly potent and brain-penetrant phosphodiesterase 10A (PDE10A) inhibitors based on the 2-oxindole scaffold were designed and synthesized. (2-Oxo-1,3-oxazolidin-3-yl)phenyl derivative 1 showed the high P-glycoprotein (P-gp) efflux (efflux ratio (ER) = 6.

Progesterone receptor antagonists, contraceptive regimens, and kits

-

Page/Page column 10, (2010/02/15)

A method of contraception is provided which involves delivery of 21 to 27 consecutive days of one or more PR antagonists in the absence of a progestin, estrogen, or other steroidal compound, followed by 1 to 7 days without any active agent. Also described is a pharmaceutically useful kit to facilitate delivery of this regimen.

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