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CHEMBRDG-BB 4024901, also known as 2-Amino-5-bromo-3-chloropyridine, is a pyridine derivative with a molecular formula of C5H4BrClN2. It features a bromine atom at the 5th position and a chlorine atom at the 3rd position on the pyridine ring. This chemical compound is widely utilized as a building block in organic synthesis and medicinal chemistry for the development of pharmaceuticals and biologically active compounds. Additionally, it serves as an intermediate in the production of agrochemicals and other fine chemicals, with its specific properties and applications varying depending on the chemical reactions it is involved in.

45806-60-8

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45806-60-8 Usage

Uses

Used in Pharmaceutical Industry:
CHEMBRDG-BB 4024901 is used as a building block for the synthesis of various pharmaceuticals and biologically active compounds. Its unique structure and functional groups enable the creation of diverse molecules with potential therapeutic applications.
Used in Medicinal Chemistry:
CHEMBRDG-BB 4024901 is employed as a key intermediate in the design and synthesis of novel drug candidates. Its presence in the molecular structure can influence the pharmacokinetic and pharmacodynamic properties of the resulting compounds, making it a valuable component in drug discovery and development processes.
Used in Agrochemical Production:
CHEMBRDG-BB 4024901 is used as an intermediate in the production of agrochemicals, contributing to the development of effective and targeted pest control solutions. Its chemical properties allow for the creation of compounds with specific modes of action, enhancing crop protection and yield.
Used in Fine Chemicals Industry:
CHEMBRDG-BB 4024901 is utilized in the synthesis of various fine chemicals, which are high-purity, specialty chemicals used in a wide range of applications, including research, diagnostics, and the production of high-value consumer products. Its versatility and reactivity make it a valuable component in the creation of these specialized compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 45806-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,8,0 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 45806-60:
(7*4)+(6*5)+(5*8)+(4*0)+(3*6)+(2*6)+(1*0)=128
128 % 10 = 8
So 45806-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H19N/c1-2-10-9-7-5-3-4-6-8-9/h9-10H,2-8H2,1H3

45806-60-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethylcycloheptanamine

1.2 Other means of identification

Product number -
Other names Cycloheptanamine,N-ethyl

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:45806-60-8 SDS

45806-60-8Upstream product

45806-60-8Downstream Products

45806-60-8Relevant academic research and scientific papers

Diethylsilane as a Powerful Reagent in Au Nanoparticle-Catalyzed Reductive Transformations

Louka, Anastasia,Kidonakis, Marios,Saridakis, Iakovos,Zantioti-Chatzouda, Elisavet-Maria,Stratakis, Manolis

, p. 3508 - 3514 (2020/06/02)

Diethylsilane (Et2SiH2), a simple and readily available dihydrosilane, that exhibits superior reactivity, as compared to monohydrosilanes, in a series of reductive transformations catalyzed by recyclable and reusable Au nanoparticles (1 mol-%) supported on TiO2. It reduces aldehydes or ketones almost instantaneously at ambient conditions. It can be used in a one pot rapid reductive amination procedure, in which premixing of aldehyde and amine is required prior to the addition of the reducing agent and the catalyst, even in a protic solvent. An unprecedented method for the synthesis of N-arylisoindolines is also shown in the reductive amination between o-phthalaldehyde and anilines. In this transformation, it is proposed that the intermediate N,2-diphenylisoindolin-1-imines are reduced stepwise to the isoindolines. Finally, Et2SiH2 readily reduces amides into amines in excellent yields and shorter reaction times relative to previously known analogous nano Au(0)-catalyzed protocols.

Herbicidally active tetrazolinones

-

, (2008/06/13)

Selective herbicidal tetrazolinones of the formula STR1 wherein X is hydrogen or halogen, Y is hydrogen or C1-4 alkyl, R1 is C1-4 alkyl, and R2 is cycloheptyl or cyclooctyl. and synergistic mixtures thereof.

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