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51781-14-7

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51781-14-7 Usage

Chemical Properties

5-(2,3-Epoxypropoxy)-3,4-dihydrocarbostyril is Off-white Solid

Uses

Different sources of media describe the Uses of 51781-14-7 differently. You can refer to the following data:
1. Used in the preparation of central nervous system depressants. Intermediate in the synthesis of Carteolol (C184450), a β-Adrenergic blocker and an antiarrhythmic agent. Carbostyril derivative.
2. 5-(2,3-Epoxypropoxy)-3,4-dihydrocarbostyril is used in the preparation of central nervous system depressants. Intermediate in the synthesis of Carteolol (C184450), a β-Adrenergic blocker and an antiarrhythmic agent. Carbostyril derivative.

Check Digit Verification of cas no

The CAS Registry Mumber 51781-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,7,8 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51781-14:
(7*5)+(6*1)+(5*7)+(4*8)+(3*1)+(2*1)+(1*4)=117
117 % 10 = 7
So 51781-14-7 is a valid CAS Registry Number.

51781-14-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(oxiran-2-ylmethoxy)-3,4-dihydro-1H-quinolin-2-one

1.2 Other means of identification

Product number -
Other names 2(1H)-Quinolinone,3,4-dihydro-5-(oxiranylmethoxy)

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:51781-14-7 SDS

51781-14-7Relevant articles and documents

Stable carteolol hydrochloride, preparation method thereof and eye medicine combination

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Paragraph 0120-0121; 0129; 0141; 0152; 0163; 0173-0174; 0185, (2017/12/06)

The invention relates to stable carteolol hydrochloride, a preparation method thereof and an eye medicine combination, in particular to a method for preparing carteolol hydrochloride. The method comprises the following steps of preparing 3-amino-2-cyclohexenone, tetrahydro-2,5(1H, 6H)-quinolinone, 5-hydroxy-3,4-dihydro-2(1H)-carbostyril and 5-(2,3-epoxypropoxy)-3,4-dihydro-2(1H)-carbostyril, and then the carteolol hydrochloride is obtained. Furthermore, the invention provides the carteolol hydrochloride crude medicine obtained according to the method, the eye medicine combination prepared by using the obtained carteolol hydrochloride as the crude medicine, and applications of the obtained carteolol hydrochloride to preparation of drugs for treating or preventing glaucoma or ocular hypertension. The method has excellent pharmaceutical characteristics, for example, the obtained crude medicine and a preparation has excellent stability.

Carbostyril compounds connected via an oxyalkyl group with a piperidine ring and having pharmaceutical utility

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, (2008/06/13)

Carbostyril derivatives of Formula I: STR1 wherein: m is 0, 1, or 2; n is 0, 1, or 2; R1 is hydrogen or lower alkyl; R2 is hydrogen, halogen, hydroxy, lower alkyl, lower alkoxy, aralkoxy, or acyloxy; R3 is hydrogen, halogen, lower alkyl, or lower alkoxy; R4 is hydrogen, hydroxy, lower alkyl, acyloxy, provided that when R4 is hydroxy or acyloxy, m and n are both 1; R5 is hydrogen or lower alkyl; and R6 is alkyl, hydroxyalkyl, alkoxyalkyl, or (dialkylamino)alkyl; and the pharmaceutically acceptable acid addition salts and N-oxides (at the carbostyril nitrogen) thereof, and compositions containing them, are useful in treating cardiovascular diseases, particularly arrhythmias. Methods of preparing intermediates, the compounds, their formulations and methods of treatment therewith are also disclosed.

CARBAMYLPIPERAZINE COMPOUNDS

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, (2008/06/13)

4-(3-Aryloxy-2-hydroxypropyl)piperazines bearing a carbamyl group in the 1-position are β-adrenergic blockers. A typical example is 1-carbamyl-4-{3-2-allyl-3-(2-carbethoxyaminoethyl)phenoxy!-2-hydroxypropyl} piperazine.

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