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21440-97-1

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21440-97-1 Usage

Uses

Antipsychotic.

Check Digit Verification of cas no

The CAS Registry Mumber 21440-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,4 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 21440-97:
(7*2)+(6*1)+(5*4)+(4*4)+(3*0)+(2*9)+(1*7)=81
81 % 10 = 1
So 21440-97-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H10BrNO2/c1-10(2)7-5-6(11)3-4-8(7)12-9(13)14-10/h3-5H,1-2H3,(H,12,13)

21440-97-1SDS

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 6-bromo-4,4-dimethyl-1H-3,1-benzoxazin-2-one

1.2 Other means of identification

Product number -
Other names 6-bromo-4,4-dimethyl-1,4-dihydro-2H-[d][3,1]-benzoxazin-2-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:21440-97-1 SDS

21440-97-1Relevant articles and documents

Acridine derivative heterocyclic aromatic compound and applicaiton of acridine derivative heterocyclic aromatic compound in organic electroluminescent component

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Paragraph 0153-0155, (2019/01/06)

The invention relates to an acridine derivative heterocyclic aromatic compound and applicaiton of the acridine derivative heterocyclic aromatic compound in an organic electroluminescent component. Theacridine derivative heterocyclic aromatic compound is represented by a general formula (1-1) or (1-2); through modification by increasing necessary electron-donating groups, hole transportability canbe improved, the triplet energy of the material can be improved, and high brightness, low voltage, high efficiency and long service life of the organic EL component can be achieved; meanwhile, the material prepared from the compound has high thermal stability, the luminescent stability of a light-emitting device can be improved significantly, and the material can be widely used as a host materialof a luminescent layer on the OLED and a display device.

SUBSTITUTED BENZO[d][1,3]OXAZIN-2(4H)-ONES AND RELATED DERIVATIVES AND THEIR USES FOR MODULATING THE PROGESTERONE RECEPTOR

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Page/Page column 11, (2009/08/16)

Compounds of formula (I), or pharmaceutically acceptable salts thereof, are provided, wherein R1-R6 and X are defined herein. Also provided are methods of preparing the compounds of formula (I), pharmaceutical compositions and kits containing a compound of formula (I), as are methods of treating endometriosis, hormone-dependent carcinomas, leiomyoma, fibroids, dysfunctional bleeding, polycystic ovary syndrome, and menopause related symptoms; methods of contraception; methods of providing hormone replacement therapy; methods of stimulating food intake; methods of synchronizing estrus; and methods of treating symptoms of premenstrual syndrome and premenstrual dysphoric disorder by administering to a mammal in need thereof a pharmaceutically effective amount of a compound of formula (I).

Synthesis and structure-activity relationship of novel 6-aryl-1,4- dihydrobenzo[d][1,3]oxazine-2-thiones as progesterone receptor modulators leading to the potent and selective nonsteroidal progesterone receptor agonist tanaproget

Fensome, Andrew,Bender, Reinhold,Chopra, Rajiv,Cohen, Jeff,Collins, Mark A.,Hudak, Valerie,Malakian, Karl,Lockhead, Susan,Olland, Andrea,Svenson, Kristine,Terefenko, Eugene A.,Unwalla, Ray J.,Wilhelm, James M.,Wolfrom, Scott,Zhu, Yuan,Zhang, Zhiming,Zhang, Puwen,Winneker, Richard C.,Wrobel, Jay

, p. 5092 - 5095 (2007/10/03)

Tanaproget represents a potential first-in-class nonsteroidal PR agonist for contraception with improved safety and side effect profiles versus currently available steroidal oral contraceptives. Additional SAR, biological activity, and structural information from a tanaproget/hPR-LBD (hPR-LBD = human progesterone receptor ligand binding domain) cocrystal structure will also be presented.

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