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5-Bromo-2-chlorobenzyl amine is a chemical compound with the molecular formula C7H7BrClN. It is a primary and secondary amine compound featuring a benzyl group substituted with a bromine atom at the 5th position and a chlorine atom at the 2nd position. 5-Bromo-2-chlorobenzyl amine is characterized by its unique structure and properties, making it a valuable building block in the synthesis of complex molecules.

1096296-85-3

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1096296-85-3 Usage

Uses

Used in Organic Synthesis:
5-Bromo-2-chlorobenzyl amine is used as a reagent and intermediate in organic synthesis for the preparation of various organic compounds. Its unique structure and properties make it a valuable building block in the synthesis of complex molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-Bromo-2-chlorobenzyl amine is utilized as a reagent and intermediate for the development of new therapeutic agents and other bioactive compounds. Its potential application in the development of new drugs highlights its importance in pharmaceutical research and development.
Used in Agrochemicals:
5-Bromo-2-chlorobenzyl amine is also used in the preparation of agrochemicals, contributing to the development of new pesticides and other agricultural chemicals.
Used in Materials Science:
5-Bromo-2-chlorobenzyl amine has potential applications in the field of materials science, where it can be used to develop new materials with specific properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1096296-85-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,6,2,9 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1096296-85:
(9*1)+(8*0)+(7*9)+(6*6)+(5*2)+(4*9)+(3*6)+(2*8)+(1*5)=193
193 % 10 = 3
So 1096296-85-3 is a valid CAS Registry Number.

1096296-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-bromo-2-chlorophenyl)methanamine

1.2 Other means of identification

Product number -
Other names (5-Bromo-2-chlorophenyl)methanamine

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:1096296-85-3 SDS

1096296-85-3Relevant academic research and scientific papers

STROBILURIN TYPE COMPOUNDS FOR COMBATING PHYTOPATHOGENIC FUNGI

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Page/Page column 101; 102, (2015/01/07)

The present invention relates to novel strobilurine type compounds I, processes for preparing these compounds, a use of compounds of the formula I and/or their agriculturally useful salts for controlling phytopathogenic fungi, to compositions comprising at least one such compound, to plant health applications, and to seeds coated with at least one such compound.

HETEROBICYCLE-SUBSTITUTED AZOLYL BENZENE FUNGICIDES

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Page/Page column 39, (2011/06/16)

Disclosed are compounds of Formula 1, including all stereoisomers, N oxides, and salts thereof, wherein Y is a 5-membered, fully or partially unsaturated heterocyclic ring containing 2-4 carbon atoms and 2-3 nitrogen atoms as ring members, the ring substi

Diazinones as P2 replacements for pyrazole-based cathepsin S inhibitors

Ameriks, Michael K.,Bembenek, Scott D.,Burdett, Matthew T.,Choong, Ingrid C.,Edwards, James P.,Gebauer, Damara,Gu, Yin,Karlsson, Lars,Purkey, Hans E.,Staker, Bart L.,Sun, Siquan,Thurmond, Robin L.,Zhu, Jian

scheme or table, p. 4060 - 4064 (2010/08/07)

A pyridazin-4-one fragment 4 (hCatS IC50 = 170 μM) discovered through Tethering was modeled into cathepsin S and predicted to overlap in S2 with the tetrahydropyridinepyrazole core of a previously disclosed series of CatS inhibitors. This fragment served as a template to design pyridazin-3-one 12 (hCatS IC50 = 430 nM), which also incorporates P3 and P5 binding elements. A crystal structure of 12 bound to Cys25Ser CatS led to the synthesis of the potent diazinone isomers 22 (hCatS IC50 = 60 nM) and 27 (hCatS IC50 = 40 nM).

ISOMERIC PURINONES AND 1H-IMIDAZOPYRIDINONES AS PKC-THETA INHIBITORS

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Page/Page column 39-40, (2009/06/27)

A chemical genus of purinones and 1H-imidazopyridinones, which are useful as PKCθ inhibitors, and their methods of use are disclosed. The genus is represented by the Formula (I).

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