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47733-27-7

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  • Benzoic acid,4-methyl-, 4-[1-hydroxy-2-[(1-methylethyl)amino]ethyl]-1,2-phenylene ester(9CI)

    Cas No: 47733-27-7

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47733-27-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 47733-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,7,3 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 47733-27:
(7*4)+(6*7)+(5*7)+(4*3)+(3*3)+(2*2)+(1*7)=137
137 % 10 = 7
So 47733-27-7 is a valid CAS Registry Number.
InChI:InChI=1/C27H29NO5/c1-17(2)28-16-23(29)22-13-14-24(32-26(30)20-9-5-18(3)6-10-20)25(15-22)33-27(31)21-11-7-19(4)8-12-21/h5-15,17,23,28-29H,16H2,1-4H3

47733-27-7SDS

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 [4-[1-hydroxy-2-(propan-2-ylamino)ethyl]-2-(4-methylbenzoyl)oxyphenyl] 4-methylbenzoate

1.2 Other means of identification

Product number -
Other names Di-para-toluoylisoproterenol

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:47733-27-7 SDS

47733-27-7Downstream Products

47733-27-7Relevant articles and documents

Isolated perfused rabbit lung as a model for intravascular and intrabronchial administration of bronchodilator drugs II: isoproterenol prodrugs

Brazzell,Kostenbauder

, p. 1274 - 1281 (2007/10/02)

The pulmonary disposition of two diester prodrugs of isoproterenol (di-p-toluoylisoproterenol and dipivaloylisoproterenol) was studied in the isolated perfused rabbit lung preparation. High-pressure liquid chromatographic methods were developed to measure diester, monoester, isoproterenol, and 3-O-methylisoproterenol from a single 1-ml perfusate sample. The prodrugs were administered directly into the circulating perfusion medium and by endotracheal instillation. Perfusate concentrations of diester, monoester, isoproterenol, and 3-O-methylisoproterenol were measured for 180 min. The diesters were rapidly eliminated from the perfusate with a subsequent increase in monoester concentrations. Isoproterenol levels were observed within minutes of prodrug administration, peaked at 60-80 min, and declined slowly thereafter. The prodrugs were rapidly absorbed following endotracheal administration with 30-50% of the diester being metabolized during the first pass through the lung.

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