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p-nitrobenzyl (6R-trans)-7-amino-3-chloro-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate monohydrochloride is a complex chemical compound that is a derivative of cyclic structures. It is characterized by the presence of multiple functional groups, including a nitrobenzyl group, an amino group, and a carboxylate group. p-nitrobenzyl (6R-trans)-7-amino-3-chloro-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate monohydrochloride also features a bicyclic structure and a chloro group. As a monohydrochloride, it has one hydrochloride group attached to its molecular structure. Its specific uses, properties, and applications are largely determined by the context of the scientific investigation or research in which it is utilized.

53483-70-8

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53483-70-8 Usage

Uses

Used in Chemical Research:
p-nitrobenzyl (6R-trans)-7-amino-3-chloro-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate monohydrochloride is used as a research compound for exploring its chemical properties and potential interactions with other molecules. Its complex structure and functional groups make it a valuable subject for studies in synthetic chemistry and chemical reactions.
Used in Biochemical Studies:
In the field of biochemistry, p-nitrobenzyl (6R-trans)-7-amino-3-chloro-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate monohydrochloride is employed as a tool to investigate its interactions with biological systems. Its unique structure and functional groups may allow it to bind to specific biological targets, making it a candidate for studies on enzyme inhibition, receptor binding, or other biochemical processes.
Used in Drug Discovery:
p-nitrobenzyl (6R-trans)-7-amino-3-chloro-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate monohydrochloride is used as a lead compound in drug discovery. Its structural features may provide a basis for the development of new pharmaceutical agents, particularly in the areas of medicinal chemistry and drug design. Researchers may use p-nitrobenzyl (6R-trans)-7-amino-3-chloro-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate monohydrochloride as a starting point for the synthesis of new drugs with potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 53483-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,8 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53483-70:
(7*5)+(6*3)+(5*4)+(4*8)+(3*3)+(2*7)+(1*0)=128
128 % 10 = 8
So 53483-70-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H12ClN3O5S.ClH/c15-9-6-24-13-10(16)12(19)17(13)11(9)14(20)23-5-7-1-3-8(4-2-7)18(21)22;/h1-4,10,13H,5-6,16H2;1H/t10-,13-;/m1./s1

53483-70-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-nitrophenyl)methyl (6R,7R)-7-amino-3-chloro-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate,hydrochloride

1.2 Other means of identification

Product number -
Other names EINECS 258-580-8

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:53483-70-8 SDS

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