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304853-89-2

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304853-89-2 Usage

Synonyms

2-amino-5-bromobenzyl alcohol

Physical Appearance

White to light yellow solid

Functional Groups

Hydroxyl (OH), amine (NH2), and bromine (Br) atom

Classification

Alcohol

Uses

Synthesis of pharmaceuticals and other organic compounds; versatile building block in organic synthesis for the production of various pharmaceutical and biologically active compounds

Safety

Handle with care, as it can be hazardous if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 304853-89-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,8,5 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 304853-89:
(8*3)+(7*0)+(6*4)+(5*8)+(4*5)+(3*3)+(2*8)+(1*9)=142
142 % 10 = 2
So 304853-89-2 is a valid CAS Registry Number.

304853-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-Amino-5-bromophenyl)-2-propanol

1.2 Other means of identification

Product number -
Other names 2-amino-5-bromophenyl-pyrid-2'-yl ketone

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:304853-89-2 SDS

304853-89-2Relevant articles and documents

Heterocyclic com pounds and organic light-emitting diode including the same

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Paragraph 0190-0195; 0254-0259, (2021/02/02)

The present invention relates to a novel heterocyclic compound and an organic light emitting element including the same as a light-emitting material and, more specifically, to a heterocyclic compound having excellent light emission properties, such as a driving voltage, luminous efficiency, and lifetime, and an organic light emitting element including the same. Since the heterocyclic compound according to the present invention is more stable compared to conventional materials and has the excellent light emission properties for a driving voltage or current efficiency, the organic light emitting element including the same can be driven with a low-voltage and light emission efficiency can be improved.

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).

1,5-Dihydro-benzo[e][1,4]oxazepin-2(1H)-ones containing a 7-(5′-cyanopyrrol-2-yl) group as nonsteroidal progesterone receptor modulators

Kern, Jeffrey C.,Terefenko, Eugene A.,Fensome, Andrew,Unwalla, Ray,Wrobel, Jay,Cohen, Jeffrey,Zhu, Yuan,Berrodin, Thomas J.,Yudt, Matthew R.,Winneker, Richard C.,Zhang, Zhiming,Zhang, Puwen

scheme or table, p. 5015 - 5017 (2009/05/30)

A series of novel 7-(5′-cyanopyrrol-2-yl) substituted benzo[1,4]oxazepin-2-ones were prepared and tested for their progesterone receptor (PR) agonist or antagonist activity in the alkaline phosphatase assay using the human T47D breast carcinoma cell line.

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