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Benzenemethanol, 2-amino-5-bromo-α-phenyl-, also known as 2-amino-5-bromo-α-phenylbenzenemethanol, is an organic compound with the chemical formula C13H12BrNO. It is a derivative of benzyl alcohol, featuring a benzene ring with a hydroxyl group (-OH) attached to the benzylic carbon, an amino group (-NH2) at the 2-position, and a bromine atom (-Br) at the 5-position. Benzenemethanol, 2-amino-5-bromo-a-phenyl- is characterized by its unique structure, which combines the properties of benzyl alcohol, amino groups, and halogenated compounds. It is used in various chemical reactions and synthesis processes, particularly in the pharmaceutical and chemical industries, due to its versatile functional groups and potential applications in the development of new drugs and other chemical products.

7141-05-1

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7141-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7141-05-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7141-05:
(6*7)+(5*1)+(4*4)+(3*1)+(2*0)+(1*5)=71
71 % 10 = 1
So 7141-05-1 is a valid CAS Registry Number.

7141-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-5-bromobenzhydrol

1.2 Other means of identification

Product number -
Other names 2-amino-5-bromo-benzhydrol

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:7141-05-1 SDS

7141-05-1Relevant academic research and scientific papers

DIHYDROQUINAZOLINONE ANALOGUES AS BRD4 INHIBITORS

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, (2014/10/15)

The present invention encompasses compounds of general formula (I) wherein the groups R1 to R4 and A1 to A5 have the meanings given in the claims and in the specification. The compounds of the invention are suitable for the treatment of diseases characterized by excessive or abnormal cell proliferation pharmaceutical preparations containing such compounds and their uses as a medicament.

DIHYDROQUINAZOLINONE ANALOGUES

-

, (2014/10/16)

The present invention encompasses compounds of general formula (I) wherein the groups R1 to R4 and A1 to A5 have the meanings given in the claims and in the specification. The compounds of the invention are suitable for the treatment of diseases characterized by excessive or abnormal cell proliferation pharmaceutical preparations containing such compounds and their uses as a medicament.

Metal-free intramolecular oxidative decarboxylative amination of primary α-amino acids with product selectivity

Yan, Yizhe,Wang, Zhiyong

supporting information; experimental part, p. 9513 - 9515 (2011/10/01)

A novel metal-free intramolecular oxidative decarboxylative coupling of primary α-amino acids with 2-aminobenzoketones under mild and neutral conditions was developed. Different quinazolines can be selectively obtained by various oxidants.

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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