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Carbamic acid, 1H-tetrazol-5-yl-, 4-nitrophenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60309-09-3

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60309-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60309-09-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,0 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60309-09:
(7*6)+(6*0)+(5*3)+(4*0)+(3*9)+(2*0)+(1*9)=93
93 % 10 = 3
So 60309-09-3 is a valid CAS Registry Number.

60309-09-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-nitrophenyl) N-(2H-tetrazol-5-yl)carbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid,1H-tetrazol-5-yl-,4-nitrophenyl ester

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:60309-09-3 SDS

60309-09-3Downstream Products

60309-09-3Relevant academic research and scientific papers

USE OF CSE INHIBITORS FOR THE TREATMENT OF CUTANEOUS INJURIES OR CONDITIONS AND SLEEP-RELATED BREATHING DISORDERS

-

Paragraph 00499, (2014/02/16)

no abstract published

CYSTATHIONINE-Υ-LYASE (CSE) INHIBITORS

-

Paragraph 00297, (2014/02/16)

Described herein are compounds and pharmaceutical compositions containing such compounds which inhibit cystathionine -γ-lyase (CSE). Also described herein are methods for using such CSE inhibitors, alone or in combination with other compounds, for treating diseases or conditions that would benefit from CSE inhibition.

Synthesis and cardiac imaging of 18F-ligands selective for β1-adrenoreceptors

Radeke, Heike S.,Purohit, Ajay,Harris, Thomas D.,Hanson, Kelley,Jones, Reinaldo,Hu, Carol,Yalamanchili, Padmaja,Hayes, Megan,Yu, Ming,Guaraldi, Mary,Kagan, Mikhail,Azure, Michael,Cdebaca, Michael,Robinson, Simon,Casebier, David

supporting information; experimental part, p. 650 - 655 (2011/11/05)

A series of potent and selective β1-adrenoreceptor ligands were identified (IC50 range, 0.04-0.25 nM; β1/ β2 selectivity range, 65-450-fold), labeled with the PET radioisotope fluorine-18 and evaluated in normal Sprague-Dawley rats. Tissue distribution studies demonstrated uptake of each radiotracers from the blood pool into the myocardium (0.48-0.62% ID/g), lung (0.63-0.97% ID/g), and liver (1.03-1.14% ID/g). Dynamic μPET imaging confirmed the in vivo dissection studies.

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